Canonical Allele Identifier: CA421821132
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873028T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903890T>C , CM000663.2:g.173903890T>C GRCh38
NC_000001.10:g.173873028T>C , CM000663.1:g.173873028T>C GRCh37
NC_000001.9:g.172139651T>C NCBI36
NG_012462.1:g.18489A>G , LRG_577:g.18489A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1394A>G MANE Select ENSP00000356671.3:p.Ter465=
ENST00000367698.3:c.1394A>G ENSP00000356671.3:p.Ter465=
ENST00000617423.4:c.779A>G ENSP00000478688.1:p.Ter260=
NM_000488.3:c.1394A>G , LRG_577t1:c.1394A>G NP_000479.1:p.Ter465=
XM_005245198.2:c.1250A>G XP_005245255.1:p.Ter417=
NM_001365052.1:c.1250A>G NP_001351981.1:p.Ter417=
NM_000488.4:c.1394A>G MANE Select NP_000479.1:p.Ter465=
NM_001365052.2:c.1250A>G NP_001351981.1:p.Ter417=
NM_001386302.1:c.1517A>G NP_001373231.1:p.Ter506=
NM_001386303.1:c.1475A>G NP_001373232.1:p.Ter492=
NM_001386304.1:c.1373A>G NP_001373233.1:p.Ter458=
NM_001386305.1:c.1337A>G NP_001373234.1:p.Ter446=
NM_001386306.1:c.1178A>G NP_001373235.1:p.Ter393=