Canonical Allele Identifier: CA1207936916
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909621T= , CM000663.2:g.173909621T= GRCh38
NC_000001.10:g.173878759T= , CM000663.1:g.173878759T= GRCh37
NC_000001.9:g.172145382T= NCBI36
NG_012462.1:g.12758A= , LRG_577:g.12758A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1084A= MANE Select ENSP00000356671.3:p.Ser362=
ENST00000367698.3:c.1084A= ENSP00000356671.3:p.Ser362=
ENST00000617423.4:c.560-2128A= ENSP00000478688.1:n.560-2128A=
NM_000488.3:c.1084A= , LRG_577t1:c.1084A= NP_000479.1:p.Ser362=
XM_005245198.2:c.940A= XP_005245255.1:p.Ser314=
NM_001365052.1:c.940A= NP_001351981.1:p.Ser314=
NM_000488.4:c.1084A= MANE Select NP_000479.1:p.Ser362=
NM_001365052.2:c.940A= NP_001351981.1:p.Ser314=
NM_001386302.1:c.1207A= NP_001373231.1:p.Ser403=
NM_001386303.1:c.1165A= NP_001373232.1:p.Ser389=
NM_001386304.1:c.1063A= NP_001373233.1:p.Ser355=
NM_001386305.1:c.1027A= NP_001373234.1:p.Ser343=
NM_001386306.1:c.868A= NP_001373235.1:p.Ser290=