Canonical Allele Identifier: CA2733627504
Gene: AKAP10 HGNC NCBI

Linked Data

dbSNP Id: rs2152409116

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19909078A>C , CM000679.2:g.19909078A>C GRCh38
NC_000017.10:g.19812391A>C , CM000679.1:g.19812391A>C GRCh37
NC_000017.9:g.19752983A>C NCBI36
NG_011493.1:g.73739T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225737.11:c.1983+103T>G MANE Select ENSP00000225737.6:n.1983+103T>G
ENST00000225737.10:c.1983+103T>G ENSP00000225737.6:n.1983+103T>G
ENST00000395536.7:c.1809+103T>G ENSP00000378907.3:n.1809+103T>G
ENST00000578898.1:c.410+103T>G
NM_007202.3:c.1983+103T>G NP_009133.2:n.1983+103T>G
XM_006721431.2:c.1835-2846T>G XP_006721494.1:n.1835-2846T>G
XM_006721432.2:c.1809+103T>G XP_006721495.1:n.1809+103T>G
XR_933969.1:n.2031+103T>G
XR_933970.1:n.1883-2846T>G
NM_001330152.1:c.1809+103T>G NP_001317081.1:n.1809+103T>G
XR_001752418.2:n.2095+103T>G
XR_933969.3:n.2014+103T>G
NM_007202.4:c.1983+103T>G MANE Select NP_009133.2:n.1983+103T>G
NM_001330152.2:c.1809+103T>G NP_001317081.1:n.1809+103T>G