Canonical Allele Identifier: CA2251265543
Gene: AKAP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19909186T= , CM000679.2:g.19909186T= GRCh38
NC_000017.10:g.19812499T= , CM000679.1:g.19812499T= GRCh37
NC_000017.9:g.19753091T= NCBI36
NG_011493.1:g.73631A=

Transcript Alleles

HGVS Amino-acid change
ENST00000225737.11:c.1978A= MANE Select ENSP00000225737.6:p.Thr660=
ENST00000225737.10:c.1978A= ENSP00000225737.6:p.Thr660=
ENST00000395536.7:c.1804A= ENSP00000378907.3:p.Thr602=
ENST00000578898.1:c.405A=
NM_007202.3:c.1978A= NP_009133.2:p.Thr660=
XM_006721431.2:c.1835-2954A= XP_006721494.1:n.1835-2954A=
XM_006721432.2:c.1804A= XP_006721495.1:p.Thr602=
XR_933969.1:n.2026A=
XR_933970.1:n.1883-2954A=
NM_001330152.1:c.1804A= NP_001317081.1:p.Thr602=
XR_001752418.2:n.2090A=
XR_933969.3:n.2009A=
NM_007202.4:c.1978A= MANE Select NP_009133.2:p.Thr660=
NM_001330152.2:c.1804A= NP_001317081.1:p.Thr602=