Canonical Allele Identifier: CA384963911
Gene: KRT6A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52886522G>C (hg19) chr12:g.52492738G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492738G>C , CM000674.2:g.52492738G>C GRCh38
NC_000012.11:g.52886522G>C , CM000674.1:g.52886522G>C GRCh37
NC_000012.10:g.51172789G>C NCBI36
NG_008298.1:g.5660C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.451C>G MANE Select ENSP00000369317.3:p.Gln151Glu
ENST00000330722.6:c.451C>G ENSP00000369317.3:p.Gln151Glu
NM_005554.3:c.451C>G NP_005545.1:p.Gln151Glu
NM_005554.4:c.451C>G MANE Select NP_005545.1:p.Gln151Glu
Search 100 bp 5'
Search 100 bp 3'