Canonical Allele Identifier: CA516679860

Gene: AKAP4

Linked Data

• gnomAD v4: X-50193087-C-T
• MyVariant Identifiers: chrX:g.49957738C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50193087C>T , CM000685.2:g.50193087C>T	GRCh38
NC_000023.10:g.49957738C>T , CM000685.1:g.49957738C>T	GRCh37
NC_000023.9:g.49844478C>T	NCBI36
NG_012552.1:g.12927G>A
NG_012552.2:g.12927G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358526.7:c.1626G>A MANE Select	ENSP00000351327.2:p.Lys542=
ENST00000358526.6:c.1626G>A	ENSP00000351327.2:p.Lys542=
ENST00000376064.7:c.1599G>A	ENSP00000365232.3:p.Lys533=
ENST00000448865.5:c.542-65G>A	ENSP00000402403.1:n.542-65G>A
ENST00000481402.5:n.1738G>A
NM_003886.2:c.1626G>A	NP_003877.2:p.Lys542=
NM_139289.1:c.1599G>A	NP_647450.1:p.Lys533=
NM_003886.3:c.1626G>A MANE Select	NP_003877.2:p.Lys542=
NM_139289.2:c.1599G>A	NP_647450.1:p.Lys533=