Canonical Allele Identifier: CA408970738
Community Standard Title: NM_001282531.3(ADNP):c.2292T>G (p.Tyr764Ter)
Gene: ADNP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.50892422A>C , CM000682.2:g.50892422A>C GRCh38
NC_000020.10:g.49508959A>C , CM000682.1:g.49508959A>C GRCh37
NC_000020.9:g.48942366A>C NCBI36
NG_034200.1:g.43569T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001282531.3:c.2292T>G MANE Select NP_001269460.1:p.Tyr764Ter
ENST00000621696.5:c.2292T>G MANE Select ENSP00000483881.1:p.Tyr764Ter
NM_001282531.1:c.2292T>G NP_001269460.1:p.Tyr764Ter
NM_001282531.2:c.2292T>G NP_001269460.1:p.Tyr764Ter
NM_001282532.1:c.2292T>G NP_001269461.1:p.Tyr764Ter
NM_001282532.2:c.2292T>G NP_001269461.1:p.Tyr764Ter
NM_001347511.1:c.2292T>G NP_001334440.1:p.Tyr764Ter
NM_001347511.2:c.2292T>G NP_001334440.1:p.Tyr764Ter
NM_015339.3:c.2292T>G NP_056154.1:p.Tyr764Ter
NM_015339.4:c.2292T>G NP_056154.1:p.Tyr764Ter
NM_015339.5:c.2292T>G NP_056154.1:p.Tyr764Ter
NM_181442.2:c.2292T>G NP_852107.1:p.Tyr764Ter
NM_181442.3:c.2292T>G NP_852107.1:p.Tyr764Ter
NM_181442.4:c.2292T>G NP_852107.1:p.Tyr764Ter
ENST00000349014.7:c.2292T>G ENSP00000342905.3:p.Tyr764Ter
ENST00000349014.8:c.2292T>G ENSP00000342905.3:p.Tyr764Ter
ENST00000371602.8:c.2292T>G ENSP00000360662.2:p.Tyr764Ter
ENST00000371602.9:c.2292T>G ENSP00000360662.2:p.Tyr764Ter
ENST00000396029.7:c.2292T>G ENSP00000379346.3:p.Tyr764Ter
ENST00000396029.8:c.2292T>G ENSP00000379346.3:p.Tyr764Ter
ENST00000396032.7:c.2292T>G ENSP00000379349.2:p.Tyr764Ter
ENST00000396032.8:c.2292T>G ENSP00000379349.2:p.Tyr764Ter
ENST00000621696.4:c.2292T>G ENSP00000483881.1:p.Tyr764Ter
ENST00000644386.1:c.202-2465T>G ENSP00000493755.1:n.202-2465T>G
ENST00000645081.1:c.1608T>G ENSP00000495540.1:p.Tyr536Ter
ENST00000673732.1:c.2508T>G ENSP00000501294.1:p.Tyr836Ter
XM_011528747.1:c.2292T>G XP_011527049.1:p.Tyr764Ter
XM_011528747.2:c.2292T>G XP_011527049.1:p.Tyr764Ter
XM_011528748.1:c.2319T>G XP_011527050.1:p.Tyr773Ter
XM_011528748.2:c.2319T>G XP_011527050.1:p.Tyr773Ter
XM_017027758.1:c.2292T>G XP_016883247.1:p.Tyr764Ter
XM_017027759.1:c.2292T>G XP_016883248.1:p.Tyr764Ter