Canonical Allele Identifier: CA384929195
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519855T>C , CM000674.2:g.52519855T>C GRCh38
NC_000012.11:g.52913639T>C , CM000674.1:g.52913639T>C GRCh37
NC_000012.10:g.51199906T>C NCBI36
NG_008297.1:g.5605A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.442A>G MANE Select ENSP00000252242.4:p.Ser148Gly
ENST00000252242.8:c.442A>G ENSP00000252242.4:p.Ser148Gly
ENST00000549420.1:c.112A>G ENSP00000447209.1:p.Ser38Gly
ENST00000551275.1:c.337A>G ENSP00000448041.1:p.Ser113Gly
ENST00000552629.5:n.540A>G
NM_000424.3:c.442A>G NP_000415.2:p.Ser148Gly
NM_000424.4:c.442A>G MANE Select NP_000415.2:p.Ser148Gly