Canonical Allele Identifier: CA384931051
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520205C>A , CM000674.2:g.52520205C>A GRCh38
NC_000012.11:g.52913989C>A , CM000674.1:g.52913989C>A GRCh37
NC_000012.10:g.51200256C>A NCBI36
NG_008297.1:g.5255G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.92G>T MANE Select ENSP00000252242.4:p.Ser31Ile
ENST00000252242.8:c.92G>T ENSP00000252242.4:p.Ser31Ile
ENST00000546577.1:c.92G>T ENSP00000449651.1:p.Ser31Ile
ENST00000549420.1:c.43+49G>T ENSP00000447209.1:n.43+49G>T
ENST00000551275.1:c.92G>T ENSP00000448041.1:p.Ser31Ile
ENST00000552629.5:n.190G>T
NM_000424.3:c.92G>T NP_000415.2:p.Ser31Ile
NM_000424.4:c.92G>T MANE Select NP_000415.2:p.Ser31Ile