Canonical Allele Identifier: CA1207937040
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909896A= , CM000663.2:g.173909896A= GRCh38
NC_000001.10:g.173879034A= , CM000663.1:g.173879034A= GRCh37
NC_000001.9:g.172145657A= NCBI36
NG_012462.1:g.12483T= , LRG_577:g.12483T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.809T= MANE Select ENSP00000356671.3:p.Leu270=
ENST00000367698.3:c.809T= ENSP00000356671.3:p.Leu270=
ENST00000487183.1:n.460T=
ENST00000617423.4:c.559+1968T= ENSP00000478688.1:n.559+1968T=
NM_000488.3:c.809T= , LRG_577t1:c.809T= NP_000479.1:p.Leu270=
XM_005245198.2:c.665T= XP_005245255.1:p.Leu222=
NM_001365052.1:c.665T= NP_001351981.1:p.Leu222=
NM_000488.4:c.809T= MANE Select NP_000479.1:p.Leu270=
NM_001365052.2:c.665T= NP_001351981.1:p.Leu222=
NM_001386302.1:c.932T= NP_001373231.1:p.Leu311=
NM_001386303.1:c.890T= NP_001373232.1:p.Leu297=
NM_001386304.1:c.788T= NP_001373233.1:p.Leu263=
NM_001386305.1:c.763-11T= NP_001373234.1:n.763-11T=
NM_001386306.1:c.593T= NP_001373235.1:p.Leu198=