Canonical Allele Identifier: CA398726133

Gene: AKAP10

Linked Data

• MyVariant Identifiers: chr17:g.19812543T>G (hg19) ; chr17:g.19909230T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909230T>G , CM000679.2:g.19909230T>G	GRCh38
NC_000017.10:g.19812543T>G , CM000679.1:g.19812543T>G	GRCh37
NC_000017.9:g.19753135T>G	NCBI36
NG_011493.1:g.73587A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1934A>C MANE Select	ENSP00000225737.6:p.Asp645Ala
ENST00000225737.10:c.1934A>C	ENSP00000225737.6:p.Asp645Ala
ENST00000395536.7:c.1760A>C	ENSP00000378907.3:p.Asp587Ala
ENST00000578898.1:c.361A>C
NM_007202.3:c.1934A>C	NP_009133.2:p.Asp645Ala
XM_006721431.2:c.1835-2998A>C	XP_006721494.1:n.1835-2998A>C
XM_006721432.2:c.1760A>C	XP_006721495.1:p.Asp587Ala
XR_933969.1:n.1982A>C
XR_933970.1:n.1883-2998A>C
NM_001330152.1:c.1760A>C	NP_001317081.1:p.Asp587Ala
XR_001752418.2:n.2046A>C
XR_933969.3:n.1965A>C
NM_007202.4:c.1934A>C MANE Select	NP_009133.2:p.Asp645Ala
NM_001330152.2:c.1760A>C	NP_001317081.1:p.Asp587Ala