Canonical Allele Identifier: CA2036520268
Gene: KRT6A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488277G= , CM000674.2:g.52488277G= GRCh38
NC_000012.11:g.52882061G= , CM000674.1:g.52882061G= GRCh37
NC_000012.10:g.51168328G= NCBI36
NG_008298.1:g.10121C=

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.1424+51C= MANE Select ENSP00000369317.3:n.1424+51C=
ENST00000330722.6:c.1424+51C= ENSP00000369317.3:n.1424+51C=
NM_005554.3:c.1424+51C= NP_005545.1:n.1424+51C=
NM_005554.4:c.1424+51C= MANE Select NP_005545.1:n.1424+51C=