Canonical Allele Identifier: CA413189870

Gene: AKAP4

Linked Data

• MyVariant Identifiers: chrX:g.49957625T>C (hg19) ; chrX:g.50192974T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50192974T>C , CM000685.2:g.50192974T>C	GRCh38
NC_000023.10:g.49957625T>C , CM000685.1:g.49957625T>C	GRCh37
NC_000023.9:g.49844365T>C	NCBI36
NG_012552.1:g.13040A>G
NG_012552.2:g.13040A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358526.7:c.1739A>G MANE Select	ENSP00000351327.2:p.Gln580Arg
ENST00000358526.6:c.1739A>G	ENSP00000351327.2:p.Gln580Arg
ENST00000376064.7:c.1712A>G	ENSP00000365232.3:p.Gln571Arg
ENST00000448865.5:c.590A>G	ENSP00000402403.1:p.Gln197Arg
ENST00000481402.5:n.1851A>G
NM_003886.2:c.1739A>G	NP_003877.2:p.Gln580Arg
NM_139289.1:c.1712A>G	NP_647450.1:p.Gln571Arg
NM_003886.3:c.1739A>G MANE Select	NP_003877.2:p.Gln580Arg
NM_139289.2:c.1712A>G	NP_647450.1:p.Gln571Arg