Canonical Allele Identifier: CA421821500
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1301351856

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903973G>A , CM000663.2:g.173903973G>A GRCh38
NC_000001.10:g.173873111G>A , CM000663.1:g.173873111G>A GRCh37
NC_000001.9:g.172139734G>A NCBI36
NG_012462.1:g.18406C>T , LRG_577:g.18406C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1311C>T MANE Select ENSP00000356671.3:p.Asn437=
ENST00000367698.3:c.1311C>T ENSP00000356671.3:p.Asn437=
ENST00000617423.4:c.696C>T ENSP00000478688.1:p.Asn232=
NM_000488.3:c.1311C>T , LRG_577t1:c.1311C>T NP_000479.1:p.Asn437=
XM_005245198.2:c.1167C>T XP_005245255.1:p.Asn389=
NM_001365052.1:c.1167C>T NP_001351981.1:p.Asn389=
NM_000488.4:c.1311C>T MANE Select NP_000479.1:p.Asn437=
NM_001365052.2:c.1167C>T NP_001351981.1:p.Asn389=
NM_001386302.1:c.1434C>T NP_001373231.1:p.Asn478=
NM_001386303.1:c.1392C>T NP_001373232.1:p.Asn464=
NM_001386304.1:c.1290C>T NP_001373233.1:p.Asn430=
NM_001386305.1:c.1254C>T NP_001373234.1:p.Asn418=
NM_001386306.1:c.1095C>T NP_001373235.1:p.Asn365=