Canonical Allele Identifier: CA384963682
Gene: KRT6A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52886497A>T (hg19) chr12:g.52492713A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492713A>T , CM000674.2:g.52492713A>T GRCh38
NC_000012.11:g.52886497A>T , CM000674.1:g.52886497A>T GRCh37
NC_000012.10:g.51172764A>T NCBI36
NG_008298.1:g.5685T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.476T>A MANE Select ENSP00000369317.3:p.Val159Glu
ENST00000330722.6:c.476T>A ENSP00000369317.3:p.Val159Glu
NM_005554.3:c.476T>A NP_005545.1:p.Val159Glu
NM_005554.4:c.476T>A MANE Select NP_005545.1:p.Val159Glu
Search 100 bp 5'
Search 100 bp 3'