Canonical Allele Identifier: CA413187838

Gene: AKAP4

Linked Data

• gnomAD v4: X-50192518-T-C
• MyVariant Identifiers: chrX:g.49957169T>C (hg19) ; chrX:g.50192518T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50192518T>C , CM000685.2:g.50192518T>C	GRCh38
NC_000023.10:g.49957169T>C , CM000685.1:g.49957169T>C	GRCh37
NC_000023.9:g.49843909T>C	NCBI36
NG_012552.1:g.13496A>G
NG_012552.2:g.13496A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358526.7:c.2195A>G MANE Select	ENSP00000351327.2:p.Asn732Ser
ENST00000358526.6:c.2195A>G	ENSP00000351327.2:p.Asn732Ser
ENST00000376064.7:c.2168A>G	ENSP00000365232.3:p.Asn723Ser
ENST00000481402.5:n.2307A>G
NM_003886.2:c.2195A>G	NP_003877.2:p.Asn732Ser
NM_139289.1:c.2168A>G	NP_647450.1:p.Asn723Ser
NM_003886.3:c.2195A>G MANE Select	NP_003877.2:p.Asn732Ser
NM_139289.2:c.2168A>G	NP_647450.1:p.Asn723Ser