Canonical Allele Identifier: CA384924026
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516763G>C , CM000674.2:g.52516763G>C GRCh38
NC_000012.11:g.52910547G>C , CM000674.1:g.52910547G>C GRCh37
NC_000012.10:g.51196814G>C NCBI36
NG_008297.1:g.8697C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1313C>G MANE Select ENSP00000252242.4:p.Ala438Gly
ENST00000252242.8:c.1313C>G ENSP00000252242.4:p.Ala438Gly
ENST00000547890.5:n.691C>G
ENST00000548409.5:c.435C>G
ENST00000549511.5:n.520C>G
ENST00000552629.5:n.1411C>G
NM_000424.3:c.1313C>G NP_000415.2:p.Ala438Gly
NM_000424.4:c.1313C>G MANE Select NP_000415.2:p.Ala438Gly