Canonical Allele Identifier: CA421821191
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873042G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903904G>A , CM000663.2:g.173903904G>A GRCh38
NC_000001.10:g.173873042G>A , CM000663.1:g.173873042G>A GRCh37
NC_000001.9:g.172139665G>A NCBI36
NG_012462.1:g.18475C>T , LRG_577:g.18475C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1380C>T MANE Select ENSP00000356671.3:p.Asn460=
ENST00000367698.3:c.1380C>T ENSP00000356671.3:p.Asn460=
ENST00000617423.4:c.765C>T ENSP00000478688.1:p.Asn255=
NM_000488.3:c.1380C>T , LRG_577t1:c.1380C>T NP_000479.1:p.Asn460=
XM_005245198.2:c.1236C>T XP_005245255.1:p.Asn412=
NM_001365052.1:c.1236C>T NP_001351981.1:p.Asn412=
NM_000488.4:c.1380C>T MANE Select NP_000479.1:p.Asn460=
NM_001365052.2:c.1236C>T NP_001351981.1:p.Asn412=
NM_001386302.1:c.1503C>T NP_001373231.1:p.Asn501=
NM_001386303.1:c.1461C>T NP_001373232.1:p.Asn487=
NM_001386304.1:c.1359C>T NP_001373233.1:p.Asn453=
NM_001386305.1:c.1323C>T NP_001373234.1:p.Asn441=
NM_001386306.1:c.1164C>T NP_001373235.1:p.Asn388=