Canonical Allele Identifier: CA398726134

Gene: AKAP10

Linked Data

• gnomAD v4: 17-19909231-C-T
• MyVariant Identifiers: chr17:g.19812544C>T (hg19) ; chr17:g.19909231C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909231C>T , CM000679.2:g.19909231C>T	GRCh38
NC_000017.10:g.19812544C>T , CM000679.1:g.19812544C>T	GRCh37
NC_000017.9:g.19753136C>T	NCBI36
NG_011493.1:g.73586G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000225737.11:c.1933G>A MANE Select	ENSP00000225737.6:p.Asp645Asn
ENST00000225737.10:c.1933G>A	ENSP00000225737.6:p.Asp645Asn
ENST00000395536.7:c.1759G>A	ENSP00000378907.3:p.Asp587Asn
ENST00000578898.1:c.360G>A
NM_007202.3:c.1933G>A	NP_009133.2:p.Asp645Asn
XM_006721431.2:c.1835-2999G>A	XP_006721494.1:n.1835-2999G>A
XM_006721432.2:c.1759G>A	XP_006721495.1:p.Asp587Asn
XR_933969.1:n.1981G>A
XR_933970.1:n.1883-2999G>A
NM_001330152.1:c.1759G>A	NP_001317081.1:p.Asp587Asn
XR_001752418.2:n.2045G>A
XR_933969.3:n.1964G>A
NM_007202.4:c.1933G>A MANE Select	NP_009133.2:p.Asp645Asn
NM_001330152.2:c.1759G>A	NP_001317081.1:p.Asp587Asn