Canonical Allele Identifier: CA264910053

Gene: KCNK13

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90149169G>A , CM000676.2:g.90149169G>A	GRCh38
NC_000014.8:g.90615513G>A , CM000676.1:g.90615513G>A	GRCh37
NC_000014.7:g.89685266G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282146.5:c.335-34942G>A MANE Select	ENSP00000282146.4:n.335-34942G>A
ENST00000282146.4:c.335-34942G>A	ENSP00000282146.4:n.335-34942G>A
NM_022054.3:c.335-34942G>A	NP_071337.2:n.335-34942G>A
NM_022054.4:c.335-34942G>A MANE Select	NP_071337.2:n.335-34942G>A