Canonical Allele Identifier: CA2036520205
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488164G= , CM000674.2:g.52488164G= GRCh38
NC_000012.11:g.52881948G= , CM000674.1:g.52881948G= GRCh37
NC_000012.10:g.51168215G= NCBI36
NG_008298.1:g.10234C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1425-61C= MANE Select ENSP00000369317.3:n.1425-61C=
ENST00000330722.6:c.1425-61C= ENSP00000369317.3:n.1425-61C=
NM_005554.3:c.1425-61C= NP_005545.1:n.1425-61C=
NM_005554.4:c.1425-61C= MANE Select NP_005545.1:n.1425-61C=