Canonical Allele Identifier: CA689834841

Gene: KRT6A

Linked Data

• dbSNP Id: rs1300987814
• gnomAD v3: 12-52488241-A-T
• gnomAD v4: 12-52488241-A-T
• MyVariant Identifiers: chr12:g.52882025A>T (hg19) ; chr12:g.52488241A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52488241A>T , CM000674.2:g.52488241A>T	GRCh38
NC_000012.11:g.52882025A>T , CM000674.1:g.52882025A>T	GRCh37
NC_000012.10:g.51168292A>T	NCBI36
NG_008298.1:g.10157T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330722.7:c.1424+87T>A MANE Select	ENSP00000369317.3:n.1424+87T>A
ENST00000330722.6:c.1424+87T>A	ENSP00000369317.3:n.1424+87T>A
NM_005554.3:c.1424+87T>A	NP_005545.1:n.1424+87T>A
NM_005554.4:c.1424+87T>A MANE Select	NP_005545.1:n.1424+87T>A