Canonical Allele Identifier: CA625113223

Gene: AKAP10

Linked Data

• dbSNP Id: rs1346469277
• gnomAD v2: 17-19812639-C-T
• gnomAD v4: 17-19909326-C-T
• MyVariant Identifiers: chr17:g.19812639C>T (hg19) ; chr17:g.19909326C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909326C>T , CM000679.2:g.19909326C>T	GRCh38
NC_000017.10:g.19812639C>T , CM000679.1:g.19812639C>T	GRCh37
NC_000017.9:g.19753231C>T	NCBI36
NG_011493.1:g.73491G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1888-50G>A MANE Select	ENSP00000225737.6:n.1888-50G>A
ENST00000225737.10:c.1888-50G>A	ENSP00000225737.6:n.1888-50G>A
ENST00000395536.7:c.1714-50G>A	ENSP00000378907.3:n.1714-50G>A
ENST00000578898.1:c.315-50G>A
ENST00000583951.1:c.199-50G>A	ENSP00000463398.1:n.199-50G>A
NM_007202.3:c.1888-50G>A	NP_009133.2:n.1888-50G>A
XM_006721431.2:c.1835-3094G>A	XP_006721494.1:n.1835-3094G>A
XM_006721432.2:c.1714-50G>A	XP_006721495.1:n.1714-50G>A
XR_933969.1:n.1936-50G>A
XR_933970.1:n.1883-3094G>A
NM_001330152.1:c.1714-50G>A	NP_001317081.1:n.1714-50G>A
XR_001752418.2:n.2000-50G>A
XR_933969.3:n.1919-50G>A
NM_007202.4:c.1888-50G>A MANE Select	NP_009133.2:n.1888-50G>A
NM_001330152.2:c.1714-50G>A	NP_001317081.1:n.1714-50G>A