Canonical Allele Identifier: CA384963277
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492665G>C , CM000674.2:g.52492665G>C GRCh38
NC_000012.11:g.52886449G>C , CM000674.1:g.52886449G>C GRCh37
NC_000012.10:g.51172716G>C NCBI36
NG_008298.1:g.5733C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.524C>G MANE Select ENSP00000369317.3:p.Ala175Gly
ENST00000330722.6:c.524C>G ENSP00000369317.3:p.Ala175Gly
ENST00000549898.5:n.45C>G
NM_005554.3:c.524C>G NP_005545.1:p.Ala175Gly
NM_005554.4:c.524C>G MANE Select NP_005545.1:p.Ala175Gly