Canonical Allele Identifier: CA8445649

Gene: AKAP10

Linked Data

• dbSNP Id: rs139686167
• ExAC: 17:19812547 T / C
• gnomAD v2: 17-19812547-T-C
• gnomAD v3: 17-19909234-T-C
• gnomAD v4: 17-19909234-T-C
• MyVariant Identifiers: chr17:g.19812547T>C (hg19) ; chr17:g.19909234T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909234T>C , CM000679.2:g.19909234T>C	GRCh38
NC_000017.10:g.19812547T>C , CM000679.1:g.19812547T>C	GRCh37
NC_000017.9:g.19753139T>C	NCBI36
NG_011493.1:g.73583A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1930A>G MANE Select	ENSP00000225737.6:p.Ser644Gly
ENST00000225737.10:c.1930A>G	ENSP00000225737.6:p.Ser644Gly
ENST00000395536.7:c.1756A>G	ENSP00000378907.3:p.Ser586Gly
ENST00000578898.1:c.357A>G
NM_007202.3:c.1930A>G	NP_009133.2:p.Ser644Gly
XM_006721431.2:c.1835-3002A>G	XP_006721494.1:n.1835-3002A>G
XM_006721432.2:c.1756A>G	XP_006721495.1:p.Ser586Gly
XR_933969.1:n.1978A>G
XR_933970.1:n.1883-3002A>G
NM_001330152.1:c.1756A>G	NP_001317081.1:p.Ser586Gly
XR_001752418.2:n.2042A>G
XR_933969.3:n.1961A>G
NM_007202.4:c.1930A>G MANE Select	NP_009133.2:p.Ser644Gly
NM_001330152.2:c.1756A>G	NP_001317081.1:p.Ser586Gly