Canonical Allele Identifier: CA1207937049
Gene: SERPINC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909933_173909934delinsTC , CM000663.2:g.173909933_173909934delinsTC GRCh38
NC_000001.10:g.173879071_173879072delinsTC , CM000663.1:g.173879071_173879072delinsTC GRCh37
NC_000001.9:g.172145694_172145695delinsTC NCBI36
NG_012462.1:g.12445_12446delinsGA , LRG_577:g.12445_12446delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.771_772delinsGA MANE Select ENSP00000356671.3:p.Trp257=
ENST00000367698.3:c.771_772delinsGA ENSP00000356671.3:p.Trp257=
ENST00000487183.1:n.422_423delinsGA
ENST00000617423.4:c.559+1930_559+1931delinsGA ENSP00000478688.1:n.559+1930_559+1931delinsGA
NM_000488.3:c.771_772delinsGA , LRG_577t1:c.771_772delinsGA NP_000479.1:p.Trp257=
XM_005245198.2:c.627_628delinsGA XP_005245255.1:p.Trp209=
NM_001365052.1:c.627_628delinsGA NP_001351981.1:p.Trp209=
NM_000488.4:c.771_772delinsGA MANE Select NP_000479.1:p.Trp257=
NM_001365052.2:c.627_628delinsGA NP_001351981.1:p.Trp209=
NM_001386302.1:c.894_895delinsGA NP_001373231.1:p.Trp298=
NM_001386303.1:c.852_853delinsGA NP_001373232.1:p.Trp284=
NM_001386304.1:c.750_751delinsGA NP_001373233.1:p.Trp250=
NM_001386305.1:c.763-49_763-48delinsGA NP_001373234.1:n.763-49_763-48delinsGA
NM_001386306.1:c.555_556delinsGA NP_001373235.1:p.Trp185=
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