Canonical Allele Identifier: CA516679396

Gene: AKAP4

Linked Data

• MyVariant Identifiers: chrX:g.49957618A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50192967A>G , CM000685.2:g.50192967A>G	GRCh38
NC_000023.10:g.49957618A>G , CM000685.1:g.49957618A>G	GRCh37
NC_000023.9:g.49844358A>G	NCBI36
NG_012552.1:g.13047T>C
NG_012552.2:g.13047T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358526.7:c.1746T>C MANE Select	ENSP00000351327.2:p.Thr582=
ENST00000358526.6:c.1746T>C	ENSP00000351327.2:p.Thr582=
ENST00000376064.7:c.1719T>C	ENSP00000365232.3:p.Thr573=
ENST00000448865.5:c.597T>C	ENSP00000402403.1:p.Thr199=
ENST00000481402.5:n.1858T>C
NM_003886.2:c.1746T>C	NP_003877.2:p.Thr582=
NM_139289.1:c.1719T>C	NP_647450.1:p.Thr573=
NM_003886.3:c.1746T>C MANE Select	NP_003877.2:p.Thr582=
NM_139289.2:c.1719T>C	NP_647450.1:p.Thr573=