Canonical Allele Identifier: CA398726236

Gene: AKAP10

Linked Data

• MyVariant Identifiers: chr17:g.19812586G>A (hg19) ; chr17:g.19909273G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19909273G>A , CM000679.2:g.19909273G>A	GRCh38
NC_000017.10:g.19812586G>A , CM000679.1:g.19812586G>A	GRCh37
NC_000017.9:g.19753178G>A	NCBI36
NG_011493.1:g.73544C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225737.11:c.1891C>T MANE Select	ENSP00000225737.6:p.Gln631Ter
ENST00000225737.10:c.1891C>T	ENSP00000225737.6:p.Gln631Ter
ENST00000395536.7:c.1717C>T	ENSP00000378907.3:p.Gln573Ter
ENST00000578898.1:c.318C>T
ENST00000583951.1:c.202C>T	ENSP00000463398.1:p.Gln68Ter
NM_007202.3:c.1891C>T	NP_009133.2:p.Gln631Ter
XM_006721431.2:c.1835-3041C>T	XP_006721494.1:n.1835-3041C>T
XM_006721432.2:c.1717C>T	XP_006721495.1:p.Gln573Ter
XR_933969.1:n.1939C>T
XR_933970.1:n.1883-3041C>T
NM_001330152.1:c.1717C>T	NP_001317081.1:p.Gln573Ter
XR_001752418.2:n.2003C>T
XR_933969.3:n.1922C>T
NM_007202.4:c.1891C>T MANE Select	NP_009133.2:p.Gln631Ter
NM_001330152.2:c.1717C>T	NP_001317081.1:p.Gln573Ter