Canonical Allele Identifier: CA1207937046
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909921T= , CM000663.2:g.173909921T= GRCh38
NC_000001.10:g.173879059T= , CM000663.1:g.173879059T= GRCh37
NC_000001.9:g.172145682T= NCBI36
NG_012462.1:g.12458A= , LRG_577:g.12458A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.784A= MANE Select ENSP00000356671.3:p.Ser262=
ENST00000367698.3:c.784A= ENSP00000356671.3:p.Ser262=
ENST00000487183.1:n.435A=
ENST00000617423.4:c.559+1943A= ENSP00000478688.1:n.559+1943A=
NM_000488.3:c.784A= , LRG_577t1:c.784A= NP_000479.1:p.Ser262=
XM_005245198.2:c.640A= XP_005245255.1:p.Ser214=
NM_001365052.1:c.640A= NP_001351981.1:p.Ser214=
NM_000488.4:c.784A= MANE Select NP_000479.1:p.Ser262=
NM_001365052.2:c.640A= NP_001351981.1:p.Ser214=
NM_001386302.1:c.907A= NP_001373231.1:p.Ser303=
NM_001386303.1:c.865A= NP_001373232.1:p.Ser289=
NM_001386304.1:c.763A= NP_001373233.1:p.Ser255=
NM_001386305.1:c.763-36A= NP_001373234.1:n.763-36A=
NM_001386306.1:c.568A= NP_001373235.1:p.Ser190=