Canonical Allele Identifier: CA237229479
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs11549952

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520196G>A , CM000674.2:g.52520196G>A GRCh38
NC_000012.11:g.52913980G>A , CM000674.1:g.52913980G>A GRCh37
NC_000012.10:g.51200247G>A NCBI36
NG_008297.1:g.5264C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.101C>T MANE Select ENSP00000252242.4:p.Ser34Phe
ENST00000252242.8:c.101C>T ENSP00000252242.4:p.Ser34Phe
ENST00000546577.1:c.101C>T ENSP00000449651.1:p.Ser34Phe
ENST00000549420.1:c.43+58C>T ENSP00000447209.1:n.43+58C>T
ENST00000551275.1:c.101C>T ENSP00000448041.1:p.Ser34Phe
ENST00000552629.5:n.199C>T
NM_000424.3:c.101C>T NP_000415.2:p.Ser34Phe
NM_000424.4:c.101C>T MANE Select NP_000415.2:p.Ser34Phe