Canonical Allele Identifier: CA540767780

Gene: CNTN4

Linked Data

• dbSNP Id: rs1353208207
• gnomAD v2: 3-3055520-TCACTCTTG-T
• gnomAD v3: 3-3013836-TCACTCTTG-T
• gnomAD v4: 3-3013836-TCACTCTTG-T
• MyVariant Identifiers: chr3:g.3055521_3055528del (hg19) ; chr3:g.3013837_3013844del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3013841_3013848del , CM000665.2:g.3013841_3013848del	GRCh38
NC_000003.11:g.3055525_3055532del , CM000665.1:g.3055525_3055532del	GRCh37
NC_000003.10:g.3030525_3030532del	NCBI36
NG_012827.1:g.918279_918286del
NG_012827.2:g.918279_918286del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000418658.6:c.1487-12261_1487-12254del MANE Select	ENSP00000396010.1:n.1487-12261_1487-12254del
ENST00000397459.6:c.503-12261_503-12254del	ENSP00000380600.2:n.503-12261_503-12254del
ENST00000397461.5:c.1487-12261_1487-12254del	ENSP00000380602.1:n.1487-12261_1487-12254del
ENST00000418658.5:c.1487-12261_1487-12254del	ENSP00000396010.1:n.1487-12261_1487-12254del
ENST00000427331.5:c.1487-12261_1487-12254del	ENSP00000413642.1:n.1487-12261_1487-12254del
ENST00000427741.5:c.*685-12261_*685-12254del	ENSP00000396719.1:n.*685-12261_*685-12254del
ENST00000430505.6:n.1684-12261_1684-12254del
NM_001206955.1:c.1487-12261_1487-12254del	NP_001193884.1:n.1487-12261_1487-12254del
NM_001206956.1:c.503-12261_503-12254del	NP_001193885.1:n.503-12261_503-12254del
NM_175607.2:c.1487-12261_1487-12254del	NP_783200.1:n.1487-12261_1487-12254del
NM_175613.2:c.503-12261_503-12254del	NP_783302.1:n.503-12261_503-12254del
XM_006713004.2:c.1487-12261_1487-12254del	XP_006713067.1:n.1487-12261_1487-12254del
XM_011533425.1:c.1487-12261_1487-12254del	XP_011531727.1:n.1487-12261_1487-12254del
XM_011533426.1:c.1487-12261_1487-12254del	XP_011531728.1:n.1487-12261_1487-12254del
XM_011533427.1:c.1487-12261_1487-12254del	XP_011531729.1:n.1487-12261_1487-12254del
XM_011533428.1:c.1487-12261_1487-12254del	XP_011531730.1:n.1487-12261_1487-12254del
XM_011533429.1:c.1487-12261_1487-12254del	XP_011531731.1:n.1487-12261_1487-12254del
XM_011533430.1:c.1487-12261_1487-12254del	XP_011531732.1:n.1487-12261_1487-12254del
XM_011533431.1:c.1454-12261_1454-12254del	XP_011531733.1:n.1454-12261_1454-12254del
NM_001350095.1:c.1487-12261_1487-12254del	NP_001337024.1:n.1487-12261_1487-12254del
XM_006713004.4:c.1487-12261_1487-12254del	XP_006713067.1:n.1487-12261_1487-12254del
XM_011533425.3:c.1487-12261_1487-12254del	XP_011531727.1:n.1487-12261_1487-12254del
XM_011533427.2:c.1487-12261_1487-12254del	XP_011531729.1:n.1487-12261_1487-12254del
XM_011533428.2:c.1487-12261_1487-12254del	XP_011531730.1:n.1487-12261_1487-12254del
XM_011533429.2:c.1487-12261_1487-12254del	XP_011531731.1:n.1487-12261_1487-12254del
XM_011533430.2:c.1487-12261_1487-12254del	XP_011531732.1:n.1487-12261_1487-12254del
XM_011533431.2:c.1454-12261_1454-12254del	XP_011531733.1:n.1454-12261_1454-12254del
XM_017005782.1:c.1487-12261_1487-12254del	XP_016861271.1:n.1487-12261_1487-12254del
XM_017005783.1:c.1487-12261_1487-12254del	XP_016861272.1:n.1487-12261_1487-12254del
XM_017005784.2:c.1487-12261_1487-12254del	XP_016861273.1:n.1487-12261_1487-12254del
XM_017005785.1:c.1487-12261_1487-12254del	XP_016861274.1:n.1487-12261_1487-12254del
XM_017005786.1:c.1487-12261_1487-12254del	XP_016861275.1:n.1487-12261_1487-12254del
XM_017005787.1:c.1487-12261_1487-12254del	XP_016861276.1:n.1487-12261_1487-12254del
NM_175607.3:c.1487-12261_1487-12254del MANE Select	NP_783200.1:n.1487-12261_1487-12254del
NM_001206955.2:c.1487-12261_1487-12254del	NP_001193884.1:n.1487-12261_1487-12254del
NM_001206956.2:c.503-12261_503-12254del	NP_001193885.1:n.503-12261_503-12254del
NM_001350095.2:c.1487-12261_1487-12254del	NP_001337024.1:n.1487-12261_1487-12254del
NM_175613.3:c.503-12261_503-12254del	NP_783302.1:n.503-12261_503-12254del