Canonical Allele Identifier: CA398726213

Gene: AKAP10

Linked Data

• COSMIC: COSM3387744
• MyVariant Identifiers: chr17:g.19812577G>C (hg19) ; chr17:g.19909264G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909264G>C , CM000679.2:g.19909264G>C	GRCh38
NC_000017.10:g.19812577G>C , CM000679.1:g.19812577G>C	GRCh37
NC_000017.9:g.19753169G>C	NCBI36
NG_011493.1:g.73553C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1900C>G MANE Select	ENSP00000225737.6:p.Leu634Val
ENST00000225737.10:c.1900C>G	ENSP00000225737.6:p.Leu634Val
ENST00000395536.7:c.1726C>G	ENSP00000378907.3:p.Leu576Val
ENST00000578898.1:c.327C>G
ENST00000583951.1:c.211C>G	ENSP00000463398.1:p.Leu71Val
NM_007202.3:c.1900C>G	NP_009133.2:p.Leu634Val
XM_006721431.2:c.1835-3032C>G	XP_006721494.1:n.1835-3032C>G
XM_006721432.2:c.1726C>G	XP_006721495.1:p.Leu576Val
XR_933969.1:n.1948C>G
XR_933970.1:n.1883-3032C>G
NM_001330152.1:c.1726C>G	NP_001317081.1:p.Leu576Val
XR_001752418.2:n.2012C>G
XR_933969.3:n.1931C>G
NM_007202.4:c.1900C>G MANE Select	NP_009133.2:p.Leu634Val
NM_001330152.2:c.1726C>G	NP_001317081.1:p.Leu576Val