Canonical Allele Identifier: CA421942785
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879033C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909895C>A , CM000663.2:g.173909895C>A GRCh38
NC_000001.10:g.173879033C>A , CM000663.1:g.173879033C>A GRCh37
NC_000001.9:g.172145656C>A NCBI36
NG_012462.1:g.12484G>T , LRG_577:g.12484G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.810G>T MANE Select ENSP00000356671.3:p.Leu270=
ENST00000367698.3:c.810G>T ENSP00000356671.3:p.Leu270=
ENST00000487183.1:n.461G>T
ENST00000617423.4:c.559+1969G>T ENSP00000478688.1:n.559+1969G>T
NM_000488.3:c.810G>T , LRG_577t1:c.810G>T NP_000479.1:p.Leu270=
XM_005245198.2:c.666G>T XP_005245255.1:p.Leu222=
NM_001365052.1:c.666G>T NP_001351981.1:p.Leu222=
NM_000488.4:c.810G>T MANE Select NP_000479.1:p.Leu270=
NM_001365052.2:c.666G>T NP_001351981.1:p.Leu222=
NM_001386302.1:c.933G>T NP_001373231.1:p.Leu311=
NM_001386303.1:c.891G>T NP_001373232.1:p.Leu297=
NM_001386304.1:c.789G>T NP_001373233.1:p.Leu263=
NM_001386305.1:c.763-10G>T NP_001373234.1:n.763-10G>T
NM_001386306.1:c.594G>T NP_001373235.1:p.Leu198=
Search 100 bp 5'
Search 100 bp 3'