Canonical Allele Identifier: CA421821152
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873033A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903895A>C , CM000663.2:g.173903895A>C GRCh38
NC_000001.10:g.173873033A>C , CM000663.1:g.173873033A>C GRCh37
NC_000001.9:g.172139656A>C NCBI36
NG_012462.1:g.18484T>G , LRG_577:g.18484T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1389T>G MANE Select ENSP00000356671.3:p.Val463=
ENST00000367698.3:c.1389T>G ENSP00000356671.3:p.Val463=
ENST00000617423.4:c.774T>G ENSP00000478688.1:p.Val258=
NM_000488.3:c.1389T>G , LRG_577t1:c.1389T>G NP_000479.1:p.Val463=
XM_005245198.2:c.1245T>G XP_005245255.1:p.Val415=
NM_001365052.1:c.1245T>G NP_001351981.1:p.Val415=
NM_000488.4:c.1389T>G MANE Select NP_000479.1:p.Val463=
NM_001365052.2:c.1245T>G NP_001351981.1:p.Val415=
NM_001386302.1:c.1512T>G NP_001373231.1:p.Val504=
NM_001386303.1:c.1470T>G NP_001373232.1:p.Val490=
NM_001386304.1:c.1368T>G NP_001373233.1:p.Val456=
NM_001386305.1:c.1332T>G NP_001373234.1:p.Val444=
NM_001386306.1:c.1173T>G NP_001373235.1:p.Val391=