Canonical Allele Identifier: CA1207936895
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909561T= , CM000663.2:g.173909561T= GRCh38
NC_000001.10:g.173878699T= , CM000663.1:g.173878699T= GRCh37
NC_000001.9:g.172145322T= NCBI36
NG_012462.1:g.12818A= , LRG_577:g.12818A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1144A= MANE Select ENSP00000356671.3:p.Lys382=
ENST00000367698.3:c.1144A= ENSP00000356671.3:p.Lys382=
ENST00000617423.4:c.560-2068A= ENSP00000478688.1:n.560-2068A=
NM_000488.3:c.1144A= , LRG_577t1:c.1144A= NP_000479.1:p.Lys382=
XM_005245198.2:c.1000A= XP_005245255.1:p.Lys334=
NM_001365052.1:c.1000A= NP_001351981.1:p.Lys334=
NM_000488.4:c.1144A= MANE Select NP_000479.1:p.Lys382=
NM_001365052.2:c.1000A= NP_001351981.1:p.Lys334=
NM_001386302.1:c.1267A= NP_001373231.1:p.Lys423=
NM_001386303.1:c.1225A= NP_001373232.1:p.Lys409=
NM_001386304.1:c.1123A= NP_001373233.1:p.Lys375=
NM_001386305.1:c.1087A= NP_001373234.1:p.Lys363=
NM_001386306.1:c.928A= NP_001373235.1:p.Lys310=