Canonical Allele Identifier: CA2636625628

Gene: AKAP10

Linked Data

• gnomAD v4: 17-19909049-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909049G>T , CM000679.2:g.19909049G>T	GRCh38
NC_000017.10:g.19812362G>T , CM000679.1:g.19812362G>T	GRCh37
NC_000017.9:g.19752954G>T	NCBI36
NG_011493.1:g.73768C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1983+132C>A MANE Select	ENSP00000225737.6:n.1983+132C>A
ENST00000225737.10:c.1983+132C>A	ENSP00000225737.6:n.1983+132C>A
ENST00000395536.7:c.1809+132C>A	ENSP00000378907.3:n.1809+132C>A
ENST00000578898.1:c.410+132C>A
NM_007202.3:c.1983+132C>A	NP_009133.2:n.1983+132C>A
XM_006721431.2:c.1835-2817C>A	XP_006721494.1:n.1835-2817C>A
XM_006721432.2:c.1809+132C>A	XP_006721495.1:n.1809+132C>A
XR_933969.1:n.2031+132C>A
XR_933970.1:n.1883-2817C>A
NM_001330152.1:c.1809+132C>A	NP_001317081.1:n.1809+132C>A
XR_001752418.2:n.2095+132C>A
XR_933969.3:n.2014+132C>A
NM_007202.4:c.1983+132C>A MANE Select	NP_009133.2:n.1983+132C>A
NM_001330152.2:c.1809+132C>A	NP_001317081.1:n.1809+132C>A