Canonical Allele Identifier: CA11435075
Gene: CNTN4 HGNC NCBI
CNTN4-AS1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.3042759A>T , CM000665.2:g.3042759A>T GRCh38
NC_000003.11:g.3084443A>T , CM000665.1:g.3084443A>T GRCh37
NC_000003.10:g.3059443A>T NCBI36
NG_012827.1:g.947197A>T
NG_012827.2:g.947197A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000418658.6:c.2512-218A>T (CNTN4) MANE Select ENSP00000396010.1:n.2512-218A>T
ENST00000397459.6:c.1528-218A>T (CNTN4) ENSP00000380600.2:n.1528-218A>T
ENST00000397461.5:c.2512-218A>T (CNTN4) ENSP00000380602.1:n.2512-218A>T
ENST00000418658.5:c.2512-218A>T (CNTN4) ENSP00000396010.1:n.2512-218A>T
ENST00000427331.5:c.2512-218A>T (CNTN4) ENSP00000413642.1:n.2512-218A>T
ENST00000427741.5:c.*1707-218A>T (CNTN4) ENSP00000396719.1:n.*1707-218A>T
ENST00000484686.1:n.762-218A>T (CNTN4)
NM_001206955.1:c.2512-218A>T (CNTN4) NP_001193884.1:n.2512-218A>T
NM_001206956.1:c.1525-218A>T (CNTN4) NP_001193885.1:n.1525-218A>T
NM_175607.2:c.2512-218A>T (CNTN4) NP_783200.1:n.2512-218A>T
NM_175613.2:c.1528-218A>T (CNTN4) NP_783302.1:n.1528-218A>T
NR_046554.1:n.180+154T>A (CNTN4-AS1)
XM_006713004.2:c.2509-218A>T (CNTN4) XP_006713067.1:n.2509-218A>T
XM_011533425.1:c.2512-218A>T (CNTN4) XP_011531727.1:n.2512-218A>T
XM_011533426.1:c.2512-218A>T (CNTN4) XP_011531728.1:n.2512-218A>T
XM_011533427.1:c.2512-218A>T (CNTN4) XP_011531729.1:n.2512-218A>T
XM_011533428.1:c.2512-218A>T (CNTN4) XP_011531730.1:n.2512-218A>T
XM_011533429.1:c.2512-218A>T (CNTN4) XP_011531731.1:n.2512-218A>T
XM_011533430.1:c.2512-218A>T (CNTN4) XP_011531732.1:n.2512-218A>T
XM_011533431.1:c.2479-218A>T (CNTN4) XP_011531733.1:n.2479-218A>T
NM_001350095.1:c.2512-218A>T (CNTN4) NP_001337024.1:n.2512-218A>T
XM_006713004.4:c.2509-218A>T (CNTN4) XP_006713067.1:n.2509-218A>T
XM_011533425.3:c.2512-218A>T (CNTN4) XP_011531727.1:n.2512-218A>T
XM_011533427.2:c.2512-218A>T (CNTN4) XP_011531729.1:n.2512-218A>T
XM_011533428.2:c.2512-218A>T (CNTN4) XP_011531730.1:n.2512-218A>T
XM_011533429.2:c.2512-218A>T (CNTN4) XP_011531731.1:n.2512-218A>T
XM_011533430.2:c.2512-218A>T (CNTN4) XP_011531732.1:n.2512-218A>T
XM_011533431.2:c.2479-218A>T (CNTN4) XP_011531733.1:n.2479-218A>T
XM_017005782.1:c.2512-218A>T (CNTN4) XP_016861271.1:n.2512-218A>T
XM_017005783.1:c.2512-218A>T (CNTN4) XP_016861272.1:n.2512-218A>T
XM_017005784.2:c.2512-218A>T (CNTN4) XP_016861273.1:n.2512-218A>T
XM_017005785.1:c.2509-218A>T (CNTN4) XP_016861274.1:n.2509-218A>T
XM_017005786.1:c.2509-218A>T (CNTN4) XP_016861275.1:n.2509-218A>T
XM_017005787.1:c.2509-218A>T (CNTN4) XP_016861276.1:n.2509-218A>T
NM_175607.3:c.2512-218A>T (CNTN4) MANE Select NP_783200.1:n.2512-218A>T
NM_001206955.2:c.2512-218A>T (CNTN4) NP_001193884.1:n.2512-218A>T
NM_001206956.2:c.1525-218A>T (CNTN4) NP_001193885.1:n.1525-218A>T
NM_001350095.2:c.2512-218A>T (CNTN4) NP_001337024.1:n.2512-218A>T
NM_175613.3:c.1528-218A>T (CNTN4) NP_783302.1:n.1528-218A>T