Canonical Allele Identifier: CA613341809

Gene: AKAP6

Linked Data

• dbSNP Id: rs1276801914
• gnomAD v2: 14-33302783-A-T
• gnomAD v3: 14-32833577-A-T
• gnomAD v4: 14-32833577-A-T
• MyVariant Identifiers: chr14:g.33302783A>T (hg19) ; chr14:g.32833577A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.32833577A>T , CM000676.2:g.32833577A>T	GRCh38
NC_000014.8:g.33302783A>T , CM000676.1:g.33302783A>T	GRCh37
NC_000014.7:g.32372534A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000280979.9:c.*3772A>T MANE Select	ENSP00000280979.4:n.*3772A>T
ENST00000280979.8:c.*3772A>T	ENSP00000280979.4:n.*3772A>T
XM_005268219.3:c.*3772A>T	XP_005268276.1:n.*3772A>T
XM_011537378.1:c.*3772A>T	XP_011535680.1:n.*3772A>T
XM_011537379.1:c.*3772A>T	XP_011535681.1:n.*3772A>T
XM_011537380.1:c.*3772A>T	XP_011535682.1:n.*3772A>T
XM_011537381.1:c.*3772A>T	XP_011535683.1:n.*3772A>T
XM_011537382.1:c.*3772A>T	XP_011535684.1:n.*3772A>T
XM_011537383.1:c.*3772A>T	XP_011535685.1:n.*3772A>T
XM_017021808.2:c.*3772A>T	XP_016877297.1:n.*3772A>T
NM_004274.5:c.*3772A>T MANE Select	NP_004265.3:n.*3772A>T