Canonical Allele Identifier: CA421942804
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1251910215

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909910G>A , CM000663.2:g.173909910G>A GRCh38
NC_000001.10:g.173879048G>A , CM000663.1:g.173879048G>A GRCh37
NC_000001.9:g.172145671G>A NCBI36
NG_012462.1:g.12469C>T , LRG_577:g.12469C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.795C>T MANE Select ENSP00000356671.3:p.Asn265=
ENST00000367698.3:c.795C>T ENSP00000356671.3:p.Asn265=
ENST00000487183.1:n.446C>T
ENST00000617423.4:c.559+1954C>T ENSP00000478688.1:n.559+1954C>T
NM_000488.3:c.795C>T , LRG_577t1:c.795C>T NP_000479.1:p.Asn265=
XM_005245198.2:c.651C>T XP_005245255.1:p.Asn217=
NM_001365052.1:c.651C>T NP_001351981.1:p.Asn217=
NM_000488.4:c.795C>T MANE Select NP_000479.1:p.Asn265=
NM_001365052.2:c.651C>T NP_001351981.1:p.Asn217=
NM_001386302.1:c.918C>T NP_001373231.1:p.Asn306=
NM_001386303.1:c.876C>T NP_001373232.1:p.Asn292=
NM_001386304.1:c.774C>T NP_001373233.1:p.Asn258=
NM_001386305.1:c.763-25C>T NP_001373234.1:n.763-25C>T
NM_001386306.1:c.579C>T NP_001373235.1:p.Asn193=