Canonical Allele Identifier: CA69141232

Gene: CNTN4

Linked Data

• dbSNP Id: rs553335229
• gnomAD v2: 3-2624855-G-A
• gnomAD v3: 3-2583171-G-A
• gnomAD v4: 3-2583171-G-A
• MyVariant Identifiers: chr3:g.2624855G>A (hg19) ; chr3:g.2583171G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.2583171G>A , CM000665.2:g.2583171G>A	GRCh38
NC_000003.11:g.2624855G>A , CM000665.1:g.2624855G>A	GRCh37
NC_000003.10:g.2599855G>A	NCBI36
NG_012827.1:g.487609G>A
NG_012827.2:g.487609G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000418658.6:c.55+11613G>A MANE Select	ENSP00000396010.1:n.55+11613G>A
ENST00000397461.5:c.55+11613G>A	ENSP00000380602.1:n.55+11613G>A
ENST00000418658.5:c.55+11613G>A	ENSP00000396010.1:n.55+11613G>A
ENST00000422330.5:c.55+11613G>A	ENSP00000408594.1:n.55+11613G>A
ENST00000427331.5:c.55+11613G>A	ENSP00000413642.1:n.55+11613G>A
ENST00000427741.5:c.55+11613G>A	ENSP00000396719.1:n.55+11613G>A
ENST00000430505.6:n.252+11613G>A
ENST00000434053.5:c.55+11613G>A	ENSP00000404085.1:n.55+11613G>A
ENST00000438282.6:n.491+11613G>A
ENST00000455083.5:c.55+11613G>A	ENSP00000390560.1:n.55+11613G>A
NM_001206955.1:c.55+11613G>A	NP_001193884.1:n.55+11613G>A
NM_175607.2:c.55+11613G>A	NP_783200.1:n.55+11613G>A
XM_006713004.2:c.55+11613G>A	XP_006713067.1:n.55+11613G>A
XM_011533425.1:c.55+11613G>A	XP_011531727.1:n.55+11613G>A
XM_011533426.1:c.55+11613G>A	XP_011531728.1:n.55+11613G>A
XM_011533427.1:c.55+11613G>A	XP_011531729.1:n.55+11613G>A
XM_011533428.1:c.55+11613G>A	XP_011531730.1:n.55+11613G>A
XM_011533429.1:c.55+11613G>A	XP_011531731.1:n.55+11613G>A
XM_011533430.1:c.55+11613G>A	XP_011531732.1:n.55+11613G>A
NM_001350095.1:c.55+11613G>A	NP_001337024.1:n.55+11613G>A
XM_006713004.4:c.55+11613G>A	XP_006713067.1:n.55+11613G>A
XM_011533425.3:c.55+11613G>A	XP_011531727.1:n.55+11613G>A
XM_011533427.2:c.55+11613G>A	XP_011531729.1:n.55+11613G>A
XM_011533428.2:c.55+11613G>A	XP_011531730.1:n.55+11613G>A
XM_011533429.2:c.55+11613G>A	XP_011531731.1:n.55+11613G>A
XM_011533430.2:c.55+11613G>A	XP_011531732.1:n.55+11613G>A
XM_017005782.1:c.55+11613G>A	XP_016861271.1:n.55+11613G>A
XM_017005783.1:c.55+11613G>A	XP_016861272.1:n.55+11613G>A
XM_017005784.2:c.55+11613G>A	XP_016861273.1:n.55+11613G>A
XM_017005785.1:c.55+11613G>A	XP_016861274.1:n.55+11613G>A
XM_017005786.1:c.55+11613G>A	XP_016861275.1:n.55+11613G>A
XM_017005787.1:c.55+11613G>A	XP_016861276.1:n.55+11613G>A
NM_175607.3:c.55+11613G>A MANE Select	NP_783200.1:n.55+11613G>A
NM_001206955.2:c.55+11613G>A	NP_001193884.1:n.55+11613G>A
NM_001350095.2:c.55+11613G>A	NP_001337024.1:n.55+11613G>A