Canonical Allele Identifier: CA1207937824
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173911905A= , CM000663.2:g.173911905A= GRCh38
NC_000001.10:g.173881043A= , CM000663.1:g.173881043A= GRCh37
NC_000001.9:g.172147666A= NCBI36
NG_012462.1:g.10474T= , LRG_577:g.10474T=

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.518T= MANE Select ENSP00000356671.3:p.Val173=
ENST00000367698.3:c.518T= ENSP00000356671.3:p.Val173=
ENST00000487183.1:n.223T=
ENST00000617423.4:c.518T= ENSP00000478688.1:p.Val173=
NM_000488.3:c.518T= , LRG_577t1:c.518T= NP_000479.1:p.Val173=
XM_005245198.2:c.374T= XP_005245255.1:p.Val125=
NM_001365052.1:c.374T= NP_001351981.1:p.Val125=
NM_000488.4:c.518T= MANE Select NP_000479.1:p.Val173=
NM_001365052.2:c.374T= NP_001351981.1:p.Val125=
NM_001386302.1:c.518T= NP_001373231.1:p.Val173=
NM_001386303.1:c.599T= NP_001373232.1:p.Val200=
NM_001386304.1:c.518T= NP_001373233.1:p.Val173=
NM_001386305.1:c.518T= NP_001373234.1:p.Val173=
NM_001386306.1:c.409-1014T= NP_001373235.1:n.409-1014T=