Canonical Allele Identifier: CA2036522673
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492561T= , CM000674.2:g.52492561T= GRCh38
NC_000012.11:g.52886345T= , CM000674.1:g.52886345T= GRCh37
NC_000012.10:g.51172612T= NCBI36
NG_008298.1:g.5837A=

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.540+88A= MANE Select ENSP00000369317.3:n.540+88A=
ENST00000330722.6:c.540+88A= ENSP00000369317.3:n.540+88A=
ENST00000549898.5:n.61+88A=
NM_005554.3:c.540+88A= NP_005545.1:n.540+88A=
NM_005554.4:c.540+88A= MANE Select NP_005545.1:n.540+88A=