Canonical Allele Identifier: CA2036520048
Gene: KRT6A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487886C= , CM000674.2:g.52487886C= GRCh38
NC_000012.11:g.52881670C= , CM000674.1:g.52881670C= GRCh37
NC_000012.10:g.51167937C= NCBI36
NG_008298.1:g.10512G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1529G= MANE Select ENSP00000369317.3:p.Gly510=
ENST00000330722.6:c.1529G= ENSP00000369317.3:p.Gly510=
NM_005554.3:c.1529G= NP_005545.1:p.Gly510=
NM_005554.4:c.1529G= MANE Select NP_005545.1:p.Gly510=
Search 100 bp 5'
Search 100 bp 3'