Canonical Allele Identifier: CA69112529

Gene: CNTN4

Linked Data

• dbSNP Id: rs17013524
• gnomAD v2: 3-2423127-T-G
• gnomAD v3: 3-2381443-T-G
• gnomAD v4: 3-2381443-T-G
• MyVariant Identifiers: chr3:g.2423127T>G (hg19) ; chr3:g.2381443T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.2381443T>G , CM000665.2:g.2381443T>G	GRCh38
NC_000003.11:g.2423127T>G , CM000665.1:g.2423127T>G	GRCh37
NC_000003.10:g.2398127T>G	NCBI36
NG_012827.1:g.285881T>G
NG_012827.2:g.285881T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000418658.6:c.-89+42210T>G MANE Select	ENSP00000396010.1:n.-89+42210T>G
ENST00000397461.5:c.-89+42210T>G	ENSP00000380602.1:n.-89+42210T>G
ENST00000418658.5:c.-89+42210T>G	ENSP00000396010.1:n.-89+42210T>G
ENST00000422330.5:c.-89+42210T>G	ENSP00000408594.1:n.-89+42210T>G
ENST00000427741.5:c.-89+42210T>G	ENSP00000396719.1:n.-89+42210T>G
ENST00000455083.5:c.-89+42210T>G	ENSP00000390560.1:n.-89+42210T>G
NM_001206955.1:c.-89+42210T>G	NP_001193884.1:n.-89+42210T>G
NM_175607.2:c.-89+42210T>G	NP_783200.1:n.-89+42210T>G
XM_006713004.2:c.-89+42210T>G	XP_006713067.1:n.-89+42210T>G
XM_011533425.1:c.-89+42210T>G	XP_011531727.1:n.-89+42210T>G
XM_011533426.1:c.-89+42210T>G	XP_011531728.1:n.-89+42210T>G
XM_011533427.1:c.-89+42210T>G	XP_011531729.1:n.-89+42210T>G
NM_001350095.1:c.-89+42210T>G	NP_001337024.1:n.-89+42210T>G
XM_006713004.4:c.-89+42210T>G	XP_006713067.1:n.-89+42210T>G
XM_011533425.3:c.-89+42210T>G	XP_011531727.1:n.-89+42210T>G
XM_011533427.2:c.-89+42210T>G	XP_011531729.1:n.-89+42210T>G
XM_017005782.1:c.-89+42210T>G	XP_016861271.1:n.-89+42210T>G
XM_017005783.1:c.-89+42210T>G	XP_016861272.1:n.-89+42210T>G
XM_017005784.2:c.-89+42210T>G	XP_016861273.1:n.-89+42210T>G
XM_017005785.1:c.-89+42210T>G	XP_016861274.1:n.-89+42210T>G
NM_175607.3:c.-89+42210T>G MANE Select	NP_783200.1:n.-89+42210T>G
NM_001206955.2:c.-89+42210T>G	NP_001193884.1:n.-89+42210T>G
NM_001350095.2:c.-89+42210T>G	NP_001337024.1:n.-89+42210T>G