Canonical Allele Identifier: CA2036522678
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492567C= , CM000674.2:g.52492567C= GRCh38
NC_000012.11:g.52886351C= , CM000674.1:g.52886351C= GRCh37
NC_000012.10:g.51172618C= NCBI36
NG_008298.1:g.5831G=

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.540+82G= MANE Select ENSP00000369317.3:n.540+82G=
ENST00000330722.6:c.540+82G= ENSP00000369317.3:n.540+82G=
ENST00000549898.5:n.61+82G=
NM_005554.3:c.540+82G= NP_005545.1:n.540+82G=
NM_005554.4:c.540+82G= MANE Select NP_005545.1:n.540+82G=