Canonical Allele Identifier: CA1341063337

Gene: CNTN4

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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