Canonical Allele Identifier: CA516679272

Gene: AKAP4

Linked Data

• MyVariant Identifiers: chrX:g.49957585G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50192934G>C , CM000685.2:g.50192934G>C	GRCh38
NC_000023.10:g.49957585G>C , CM000685.1:g.49957585G>C	GRCh37
NC_000023.9:g.49844325G>C	NCBI36
NG_012552.1:g.13080C>G
NG_012552.2:g.13080C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358526.7:c.1779C>G MANE Select	ENSP00000351327.2:p.Ala593=
ENST00000358526.6:c.1779C>G	ENSP00000351327.2:p.Ala593=
ENST00000376064.7:c.1752C>G	ENSP00000365232.3:p.Ala584=
ENST00000448865.5:c.630C>G	ENSP00000402403.1:p.Ala210=
ENST00000481402.5:n.1891C>G
NM_003886.2:c.1779C>G	NP_003877.2:p.Ala593=
NM_139289.1:c.1752C>G	NP_647450.1:p.Ala584=
NM_003886.3:c.1779C>G MANE Select	NP_003877.2:p.Ala593=
NM_139289.2:c.1752C>G	NP_647450.1:p.Ala584=