Canonical Allele Identifier: CA413189123

Gene: AKAP4

Linked Data

• dbSNP Id: rs1935130303
• gnomAD v3: X-50192808-C-G
• gnomAD v4: X-50192808-C-G
• MyVariant Identifiers: chrX:g.49957459C>G (hg19) ; chrX:g.50192808C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50192808C>G , CM000685.2:g.50192808C>G	GRCh38
NC_000023.10:g.49957459C>G , CM000685.1:g.49957459C>G	GRCh37
NC_000023.9:g.49844199C>G	NCBI36
NG_012552.1:g.13206G>C
NG_012552.2:g.13206G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358526.7:c.1905G>C MANE Select	ENSP00000351327.2:p.Gln635His
ENST00000358526.6:c.1905G>C	ENSP00000351327.2:p.Gln635His
ENST00000376064.7:c.1878G>C	ENSP00000365232.3:p.Gln626His
ENST00000481402.5:n.2017G>C
NM_003886.2:c.1905G>C	NP_003877.2:p.Gln635His
NM_139289.1:c.1878G>C	NP_647450.1:p.Gln626His
NM_003886.3:c.1905G>C MANE Select	NP_003877.2:p.Gln635His
NM_139289.2:c.1878G>C	NP_647450.1:p.Gln626His