Canonical Allele Identifier: CA635768617

Gene: ADNP

Linked Data

• dbSNP Id: rs1271519943
• gnomAD v2: 20-49520388-T-C
• gnomAD v3: 20-50903851-T-C
• gnomAD v4: 20-50903851-T-C
• MyVariant Identifiers: chr20:g.49520388T>C (hg19) ; chr20:g.50903851T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.50903851T>C , CM000682.2:g.50903851T>C	GRCh38
NC_000020.10:g.49520388T>C , CM000682.1:g.49520388T>C	GRCh37
NC_000020.9:g.48953795T>C	NCBI36
NG_034200.1:g.32140A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000349014.8:c.108+38A>G	ENSP00000342905.3:n.108+38A>G
ENST00000371602.9:c.108+38A>G	ENSP00000360662.2:n.108+38A>G
ENST00000396029.8:c.108+38A>G	ENSP00000379346.3:n.108+38A>G
ENST00000396032.8:c.108+38A>G	ENSP00000379349.2:n.108+38A>G
ENST00000621696.5:c.108+38A>G MANE Select	ENSP00000483881.1:n.108+38A>G
ENST00000642364.1:n.86-1742A>G
ENST00000644386.1:c.108+38A>G	ENSP00000493755.1:n.108+38A>G
ENST00000645081.1:c.-576-1742A>G	ENSP00000495540.1:n.-576-1742A>G
ENST00000673732.1:c.324+38A>G	ENSP00000501294.1:n.324+38A>G
ENST00000349014.7:c.108+38A>G	ENSP00000342905.3:n.108+38A>G
ENST00000371602.8:c.108+38A>G	ENSP00000360662.2:n.108+38A>G
ENST00000396029.7:c.108+38A>G	ENSP00000379346.3:n.108+38A>G
ENST00000396032.7:c.108+38A>G	ENSP00000379349.2:n.108+38A>G
ENST00000534467.1:c.108+38A>G	ENSP00000436181.1:n.108+38A>G
ENST00000621696.4:c.108+38A>G	ENSP00000483881.1:n.108+38A>G
NM_001282531.1:c.108+38A>G	NP_001269460.1:n.108+38A>G
NM_001282532.1:c.108+38A>G	NP_001269461.1:n.108+38A>G
NM_015339.3:c.108+38A>G	NP_056154.1:n.108+38A>G
NM_181442.2:c.108+38A>G	NP_852107.1:n.108+38A>G
XM_011528747.1:c.108+38A>G	XP_011527049.1:n.108+38A>G
XM_011528748.1:c.135+38A>G	XP_011527050.1:n.135+38A>G
NM_001282531.2:c.108+38A>G	NP_001269460.1:n.108+38A>G
NM_001347511.1:c.108+38A>G	NP_001334440.1:n.108+38A>G
NM_015339.4:c.108+38A>G	NP_056154.1:n.108+38A>G
NM_181442.3:c.108+38A>G	NP_852107.1:n.108+38A>G
XM_011528747.2:c.108+38A>G	XP_011527049.1:n.108+38A>G
XM_011528748.2:c.135+38A>G	XP_011527050.1:n.135+38A>G
XM_017027758.1:c.108+38A>G	XP_016883247.1:n.108+38A>G
XM_017027759.1:c.108+38A>G	XP_016883248.1:n.108+38A>G
NM_001282531.3:c.108+38A>G MANE Select	NP_001269460.1:n.108+38A>G
NM_001347511.2:c.108+38A>G	NP_001334440.1:n.108+38A>G
NM_015339.5:c.108+38A>G	NP_056154.1:n.108+38A>G
NM_181442.4:c.108+38A>G	NP_852107.1:n.108+38A>G
NM_001282532.2:c.108+38A>G	NP_001269461.1:n.108+38A>G