Canonical Allele Identifier: CA6582942
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs368584130

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520235G>A , CM000674.2:g.52520235G>A GRCh38
NC_000012.11:g.52914019G>A , CM000674.1:g.52914019G>A GRCh37
NC_000012.10:g.51200286G>A NCBI36
NG_008297.1:g.5225C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.62C>T MANE Select ENSP00000252242.4:p.Ser21Phe
ENST00000252242.8:c.62C>T ENSP00000252242.4:p.Ser21Phe
ENST00000546577.1:c.62C>T ENSP00000449651.1:p.Ser21Phe
ENST00000549420.1:c.43+19C>T ENSP00000447209.1:n.43+19C>T
ENST00000551275.1:c.62C>T ENSP00000448041.1:p.Ser21Phe
ENST00000552629.5:n.160C>T
NM_000424.3:c.62C>T NP_000415.2:p.Ser21Phe
NM_000424.4:c.62C>T MANE Select NP_000415.2:p.Ser21Phe