Canonical Allele Identifier: CA2036522683
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492578T= , CM000674.2:g.52492578T= GRCh38
NC_000012.11:g.52886362T= , CM000674.1:g.52886362T= GRCh37
NC_000012.10:g.51172629T= NCBI36
NG_008298.1:g.5820A=

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.540+71A= MANE Select ENSP00000369317.3:n.540+71A=
ENST00000330722.6:c.540+71A= ENSP00000369317.3:n.540+71A=
ENST00000549898.5:n.61+71A=
NM_005554.3:c.540+71A= NP_005545.1:n.540+71A=
NM_005554.4:c.540+71A= MANE Select NP_005545.1:n.540+71A=