Canonical Allele Identifier: CA398726128

Gene: AKAP10

Linked Data

• gnomAD v4: 17-19909228-T-A
• MyVariant Identifiers: chr17:g.19812541T>A (hg19) ; chr17:g.19909228T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909228T>A , CM000679.2:g.19909228T>A	GRCh38
NC_000017.10:g.19812541T>A , CM000679.1:g.19812541T>A	GRCh37
NC_000017.9:g.19753133T>A	NCBI36
NG_011493.1:g.73589A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1936A>T MANE Select	ENSP00000225737.6:p.Ile646Phe
ENST00000225737.10:c.1936A>T	ENSP00000225737.6:p.Ile646Phe
ENST00000395536.7:c.1762A>T	ENSP00000378907.3:p.Ile588Phe
ENST00000578898.1:c.363A>T
NM_007202.3:c.1936A>T	NP_009133.2:p.Ile646Phe
XM_006721431.2:c.1835-2996A>T	XP_006721494.1:n.1835-2996A>T
XM_006721432.2:c.1762A>T	XP_006721495.1:p.Ile588Phe
XR_933969.1:n.1984A>T
XR_933970.1:n.1883-2996A>T
NM_001330152.1:c.1762A>T	NP_001317081.1:p.Ile588Phe
XR_001752418.2:n.2048A>T
XR_933969.3:n.1967A>T
NM_007202.4:c.1936A>T MANE Select	NP_009133.2:p.Ile646Phe
NM_001330152.2:c.1762A>T	NP_001317081.1:p.Ile588Phe