Canonical Allele Identifier: CA421943003
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878889G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909751G>T , CM000663.2:g.173909751G>T GRCh38
NC_000001.10:g.173878889G>T , CM000663.1:g.173878889G>T GRCh37
NC_000001.9:g.172145512G>T NCBI36
NG_012462.1:g.12628C>A , LRG_577:g.12628C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.954C>A MANE Select ENSP00000356671.3:p.Pro318=
ENST00000367698.3:c.954C>A ENSP00000356671.3:p.Pro318=
ENST00000487183.1:n.605C>A
ENST00000617423.4:c.559+2113C>A ENSP00000478688.1:n.559+2113C>A
NM_000488.3:c.954C>A , LRG_577t1:c.954C>A NP_000479.1:p.Pro318=
XM_005245198.2:c.810C>A XP_005245255.1:p.Pro270=
NM_001365052.1:c.810C>A NP_001351981.1:p.Pro270=
NM_000488.4:c.954C>A MANE Select NP_000479.1:p.Pro318=
NM_001365052.2:c.810C>A NP_001351981.1:p.Pro270=
NM_001386302.1:c.1077C>A NP_001373231.1:p.Pro359=
NM_001386303.1:c.1035C>A NP_001373232.1:p.Pro345=
NM_001386304.1:c.933C>A NP_001373233.1:p.Pro311=
NM_001386305.1:c.897C>A NP_001373234.1:p.Pro299=
NM_001386306.1:c.738C>A NP_001373235.1:p.Pro246=