Canonical Allele Identifier: CA421942873
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878784G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909646G>A , CM000663.2:g.173909646G>A GRCh38
NC_000001.10:g.173878784G>A , CM000663.1:g.173878784G>A GRCh37
NC_000001.9:g.172145407G>A NCBI36
NG_012462.1:g.12733C>T , LRG_577:g.12733C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1059C>T MANE Select ENSP00000356671.3:p.Pro353=
ENST00000367698.3:c.1059C>T ENSP00000356671.3:p.Pro353=
ENST00000617423.4:c.560-2153C>T ENSP00000478688.1:p.=
NM_000488.3:c.1059C>T , LRG_577t1:c.1059C>T NP_000479.1:p.Pro353=
XM_005245198.2:c.915C>T XP_005245255.1:p.Pro305=
NM_001365052.1:c.915C>T NP_001351981.1:p.Pro305=
NM_000488.4:c.1059C>T MANE Select NP_000479.1:p.Pro353=
NM_001365052.2:c.915C>T NP_001351981.1:p.Pro305=
NM_001386302.1:c.1182C>T NP_001373231.1:p.Pro394=
NM_001386303.1:c.1140C>T NP_001373232.1:p.Pro380=
NM_001386304.1:c.1038C>T NP_001373233.1:p.Pro346=
NM_001386305.1:c.1002C>T NP_001373234.1:p.Pro334=
NM_001386306.1:c.843C>T NP_001373235.1:p.Pro281=