Canonical Allele Identifier: CA413187697

Gene: AKAP4

Linked Data

• gnomAD v4: X-50192481-A-T
• MyVariant Identifiers: chrX:g.49957132A>T (hg19) ; chrX:g.50192481A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50192481A>T , CM000685.2:g.50192481A>T	GRCh38
NC_000023.10:g.49957132A>T , CM000685.1:g.49957132A>T	GRCh37
NC_000023.9:g.49843872A>T	NCBI36
NG_012552.1:g.13533T>A
NG_012552.2:g.13533T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358526.7:c.2232T>A MANE Select	ENSP00000351327.2:p.Ser744Arg
ENST00000358526.6:c.2232T>A	ENSP00000351327.2:p.Ser744Arg
ENST00000376064.7:c.2205T>A	ENSP00000365232.3:p.Ser735Arg
ENST00000481402.5:n.2344T>A
NM_003886.2:c.2232T>A	NP_003877.2:p.Ser744Arg
NM_139289.1:c.2205T>A	NP_647450.1:p.Ser735Arg
NM_003886.3:c.2232T>A MANE Select	NP_003877.2:p.Ser744Arg
NM_139289.2:c.2205T>A	NP_647450.1:p.Ser735Arg