Canonical Allele Identifier: CA413190078

Gene: AKAP4

Linked Data

• MyVariant Identifiers: chrX:g.49957675T>C (hg19) ; chrX:g.50193024T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50193024T>C , CM000685.2:g.50193024T>C	GRCh38
NC_000023.10:g.49957675T>C , CM000685.1:g.49957675T>C	GRCh37
NC_000023.9:g.49844415T>C	NCBI36
NG_012552.1:g.12990A>G
NG_012552.2:g.12990A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358526.7:c.1689A>G MANE Select	ENSP00000351327.2:p.Lys563=
ENST00000358526.6:c.1689A>G	ENSP00000351327.2:p.Lys563=
ENST00000376064.7:c.1662A>G	ENSP00000365232.3:p.Lys554=
ENST00000448865.5:c.542-2A>G	ENSP00000402403.1:n.542-2A>G
ENST00000481402.5:n.1801A>G
NM_003886.2:c.1689A>G	NP_003877.2:p.Lys563=
NM_139289.1:c.1662A>G	NP_647450.1:p.Lys554=
NM_003886.3:c.1689A>G MANE Select	NP_003877.2:p.Lys563=
NM_139289.2:c.1662A>G	NP_647450.1:p.Lys554=