Canonical Allele Identifier: CA1207937052
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909939G= , CM000663.2:g.173909939G= GRCh38
NC_000001.10:g.173879077G= , CM000663.1:g.173879077G= GRCh37
NC_000001.9:g.172145700G= NCBI36
NG_012462.1:g.12440C= , LRG_577:g.12440C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.766C= MANE Select ENSP00000356671.3:p.Leu256=
ENST00000367698.3:c.766C= ENSP00000356671.3:p.Leu256=
ENST00000487183.1:n.417C=
ENST00000617423.4:c.559+1925C= ENSP00000478688.1:n.559+1925C=
NM_000488.3:c.766C= , LRG_577t1:c.766C= NP_000479.1:p.Leu256=
XM_005245198.2:c.622C= XP_005245255.1:p.Leu208=
NM_001365052.1:c.622C= NP_001351981.1:p.Leu208=
NM_000488.4:c.766C= MANE Select NP_000479.1:p.Leu256=
NM_001365052.2:c.622C= NP_001351981.1:p.Leu208=
NM_001386302.1:c.889C= NP_001373231.1:p.Leu297=
NM_001386303.1:c.847C= NP_001373232.1:p.Leu283=
NM_001386304.1:c.745C= NP_001373233.1:p.Leu249=
NM_001386305.1:c.763-54C= NP_001373234.1:n.763-54C=
NM_001386306.1:c.550C= NP_001373235.1:p.Leu184=