Canonical Allele Identifier: CA479848515
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs1348648817

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520207G>A , CM000674.2:g.52520207G>A GRCh38
NC_000012.11:g.52913991G>A , CM000674.1:g.52913991G>A GRCh37
NC_000012.10:g.51200258G>A NCBI36
NG_008297.1:g.5253C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.90C>T MANE Select ENSP00000252242.4:p.Thr30=
ENST00000252242.8:c.90C>T ENSP00000252242.4:p.Thr30=
ENST00000546577.1:c.90C>T ENSP00000449651.1:p.Thr30=
ENST00000549420.1:c.43+47C>T ENSP00000447209.1:n.43+47C>T
ENST00000551275.1:c.90C>T ENSP00000448041.1:p.Thr30=
ENST00000552629.5:n.188C>T
NM_000424.3:c.90C>T NP_000415.2:p.Thr30=
NM_000424.4:c.90C>T MANE Select NP_000415.2:p.Thr30=