Canonical Allele Identifier: CA413189939

Gene: AKAP4

Linked Data

• MyVariant Identifiers: chrX:g.49957643G>A (hg19) ; chrX:g.50192992G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50192992G>A , CM000685.2:g.50192992G>A	GRCh38
NC_000023.10:g.49957643G>A , CM000685.1:g.49957643G>A	GRCh37
NC_000023.9:g.49844383G>A	NCBI36
NG_012552.1:g.13022C>T
NG_012552.2:g.13022C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358526.7:c.1721C>T MANE Select	ENSP00000351327.2:p.Thr574Ile
ENST00000358526.6:c.1721C>T	ENSP00000351327.2:p.Thr574Ile
ENST00000376064.7:c.1694C>T	ENSP00000365232.3:p.Thr565Ile
ENST00000448865.5:c.572C>T	ENSP00000402403.1:p.Thr191Ile
ENST00000481402.5:n.1833C>T
NM_003886.2:c.1721C>T	NP_003877.2:p.Thr574Ile
NM_139289.1:c.1694C>T	NP_647450.1:p.Thr565Ile
NM_003886.3:c.1721C>T MANE Select	NP_003877.2:p.Thr574Ile
NM_139289.2:c.1694C>T	NP_647450.1:p.Thr565Ile