Canonical Allele Identifier: CA2618930497
Gene: KRT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492594C>T , CM000674.2:g.52492594C>T GRCh38
NC_000012.11:g.52886378C>T , CM000674.1:g.52886378C>T GRCh37
NC_000012.10:g.51172645C>T NCBI36
NG_008298.1:g.5804G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.540+55G>A MANE Select ENSP00000369317.3:n.540+55G>A
ENST00000330722.6:c.540+55G>A ENSP00000369317.3:n.540+55G>A
ENST00000549898.5:n.61+55G>A
NM_005554.3:c.540+55G>A NP_005545.1:n.540+55G>A
NM_005554.4:c.540+55G>A MANE Select NP_005545.1:n.540+55G>A