Canonical Allele Identifier: CA398726179

Gene: AKAP10

Linked Data

• MyVariant Identifiers: chr17:g.19812562C>G (hg19) ; chr17:g.19909249C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909249C>G , CM000679.2:g.19909249C>G	GRCh38
NC_000017.10:g.19812562C>G , CM000679.1:g.19812562C>G	GRCh37
NC_000017.9:g.19753154C>G	NCBI36
NG_011493.1:g.73568G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1915G>C MANE Select	ENSP00000225737.6:p.Ala639Pro
ENST00000225737.10:c.1915G>C	ENSP00000225737.6:p.Ala639Pro
ENST00000395536.7:c.1741G>C	ENSP00000378907.3:p.Ala581Pro
ENST00000578898.1:c.342G>C
ENST00000583951.1:c.226G>C	ENSP00000463398.1:p.Ala76Pro
NM_007202.3:c.1915G>C	NP_009133.2:p.Ala639Pro
XM_006721431.2:c.1835-3017G>C	XP_006721494.1:n.1835-3017G>C
XM_006721432.2:c.1741G>C	XP_006721495.1:p.Ala581Pro
XR_933969.1:n.1963G>C
XR_933970.1:n.1883-3017G>C
NM_001330152.1:c.1741G>C	NP_001317081.1:p.Ala581Pro
XR_001752418.2:n.2027G>C
XR_933969.3:n.1946G>C
NM_007202.4:c.1915G>C MANE Select	NP_009133.2:p.Ala639Pro
NM_001330152.2:c.1741G>C	NP_001317081.1:p.Ala581Pro