Canonical Allele Identifier: CA2227668

Gene: CNTN4 CNTN4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3040141T>C , CM000665.2:g.3040141T>C	GRCh38
NC_000003.11:g.3081825T>C , CM000665.1:g.3081825T>C	GRCh37
NC_000003.10:g.3056825T>C	NCBI36
NG_012827.1:g.944579T>C
NG_012827.2:g.944579T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000418658.6:c.2268T>C (CNTN4) MANE Select	ENSP00000396010.1:p.Asp756=
ENST00000397459.6:c.1284T>C (CNTN4)	ENSP00000380600.2:p.Asp428=
ENST00000397461.5:c.2268T>C (CNTN4)	ENSP00000380602.1:p.Asp756=
ENST00000418658.5:c.2268T>C (CNTN4)	ENSP00000396010.1:p.Asp756=
ENST00000427331.5:c.2268T>C (CNTN4)	ENSP00000413642.1:p.Asp756=
ENST00000427741.5:c.*1463T>C (CNTN4)	ENSP00000396719.1:n.*1463T>C
ENST00000484686.1:n.518T>C (CNTN4)
NM_001206955.1:c.2268T>C (CNTN4)	NP_001193884.1:p.Asp756=
NM_001206956.1:c.1281T>C (CNTN4)	NP_001193885.1:p.Asp427=
NM_175607.2:c.2268T>C (CNTN4)	NP_783200.1:p.Asp756=
NM_175613.2:c.1284T>C (CNTN4)	NP_783302.1:p.Asp428=
NR_046554.1:n.532A>G (CNTN4-AS1)
XM_006713004.2:c.2265T>C (CNTN4)	XP_006713067.1:p.Asp755=
XM_011533425.1:c.2268T>C (CNTN4)	XP_011531727.1:p.Asp756=
XM_011533426.1:c.2268T>C (CNTN4)	XP_011531728.1:p.Asp756=
XM_011533427.1:c.2268T>C (CNTN4)	XP_011531729.1:p.Asp756=
XM_011533428.1:c.2268T>C (CNTN4)	XP_011531730.1:p.Asp756=
XM_011533429.1:c.2268T>C (CNTN4)	XP_011531731.1:p.Asp756=
XM_011533430.1:c.2268T>C (CNTN4)	XP_011531732.1:p.Asp756=
XM_011533431.1:c.2235T>C (CNTN4)	XP_011531733.1:p.Asp745=
NM_001350095.1:c.2268T>C (CNTN4)	NP_001337024.1:p.Asp756=
XM_006713004.4:c.2265T>C (CNTN4)	XP_006713067.1:p.Asp755=
XM_011533425.3:c.2268T>C (CNTN4)	XP_011531727.1:p.Asp756=
XM_011533427.2:c.2268T>C (CNTN4)	XP_011531729.1:p.Asp756=
XM_011533428.2:c.2268T>C (CNTN4)	XP_011531730.1:p.Asp756=
XM_011533429.2:c.2268T>C (CNTN4)	XP_011531731.1:p.Asp756=
XM_011533430.2:c.2268T>C (CNTN4)	XP_011531732.1:p.Asp756=
XM_011533431.2:c.2235T>C (CNTN4)	XP_011531733.1:p.Asp745=
XM_017005782.1:c.2268T>C (CNTN4)	XP_016861271.1:p.Asp756=
XM_017005783.1:c.2268T>C (CNTN4)	XP_016861272.1:p.Asp756=
XM_017005784.2:c.2268T>C (CNTN4)	XP_016861273.1:p.Asp756=
XM_017005785.1:c.2265T>C (CNTN4)	XP_016861274.1:p.Asp755=
XM_017005786.1:c.2265T>C (CNTN4)	XP_016861275.1:p.Asp755=
XM_017005787.1:c.2265T>C (CNTN4)	XP_016861276.1:p.Asp755=
NM_175607.3:c.2268T>C (CNTN4) MANE Select	NP_783200.1:p.Asp756=
NM_001206955.2:c.2268T>C (CNTN4)	NP_001193884.1:p.Asp756=
NM_001206956.2:c.1281T>C (CNTN4)	NP_001193885.1:p.Asp427=
NM_001350095.2:c.2268T>C (CNTN4)	NP_001337024.1:p.Asp756=
NM_175613.3:c.1284T>C (CNTN4)	NP_783302.1:p.Asp428=