Canonical Allele Identifier: CA1207937037
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909887T= , CM000663.2:g.173909887T= GRCh38
NC_000001.10:g.173879025T= , CM000663.1:g.173879025T= GRCh37
NC_000001.9:g.172145648T= NCBI36
NG_012462.1:g.12492A= , LRG_577:g.12492A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.818A= MANE Select ENSP00000356671.3:p.Lys273=
ENST00000367698.3:c.818A= ENSP00000356671.3:p.Lys273=
ENST00000487183.1:n.469A=
ENST00000617423.4:c.559+1977A= ENSP00000478688.1:n.559+1977A=
NM_000488.3:c.818A= , LRG_577t1:c.818A= NP_000479.1:p.Lys273=
XM_005245198.2:c.674A= XP_005245255.1:p.Lys225=
NM_001365052.1:c.674A= NP_001351981.1:p.Lys225=
NM_000488.4:c.818A= MANE Select NP_000479.1:p.Lys273=
NM_001365052.2:c.674A= NP_001351981.1:p.Lys225=
NM_001386302.1:c.941A= NP_001373231.1:p.Lys314=
NM_001386303.1:c.899A= NP_001373232.1:p.Lys300=
NM_001386304.1:c.797A= NP_001373233.1:p.Lys266=
NM_001386305.1:c.763-2A= NP_001373234.1:n.763-2A=
NM_001386306.1:c.602A= NP_001373235.1:p.Lys201=