Canonical Allele Identifier: CA413190303

Gene: AKAP4

Linked Data

• dbSNP Id: rs1167483575
• gnomAD v3: X-50193076-A-T
• gnomAD v4: X-50193076-A-T
• MyVariant Identifiers: chrX:g.49957727A>T (hg19) ; chrX:g.50193076A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50193076A>T , CM000685.2:g.50193076A>T	GRCh38
NC_000023.10:g.49957727A>T , CM000685.1:g.49957727A>T	GRCh37
NC_000023.9:g.49844467A>T	NCBI36
NG_012552.1:g.12938T>A
NG_012552.2:g.12938T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358526.7:c.1637T>A MANE Select	ENSP00000351327.2:p.Val546Asp
ENST00000358526.6:c.1637T>A	ENSP00000351327.2:p.Val546Asp
ENST00000376064.7:c.1610T>A	ENSP00000365232.3:p.Val537Asp
ENST00000448865.5:c.542-54T>A	ENSP00000402403.1:n.542-54T>A
ENST00000481402.5:n.1749T>A
NM_003886.2:c.1637T>A	NP_003877.2:p.Val546Asp
NM_139289.1:c.1610T>A	NP_647450.1:p.Val537Asp
NM_003886.3:c.1637T>A MANE Select	NP_003877.2:p.Val546Asp
NM_139289.2:c.1610T>A	NP_647450.1:p.Val537Asp