Canonical Allele Identifier: CA2036522680
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492570G= , CM000674.2:g.52492570G= GRCh38
NC_000012.11:g.52886354G= , CM000674.1:g.52886354G= GRCh37
NC_000012.10:g.51172621G= NCBI36
NG_008298.1:g.5828C=

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.540+79C= MANE Select ENSP00000369317.3:n.540+79C=
ENST00000330722.6:c.540+79C= ENSP00000369317.3:n.540+79C=
ENST00000549898.5:n.61+79C=
NM_005554.3:c.540+79C= NP_005545.1:n.540+79C=
NM_005554.4:c.540+79C= MANE Select NP_005545.1:n.540+79C=