Canonical Allele Identifier: CA2227178

Gene: CNTN4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.2887190G>C , CM000665.2:g.2887190G>C	GRCh38
NC_000003.11:g.2928874G>C , CM000665.1:g.2928874G>C	GRCh37
NC_000003.10:g.2903874G>C	NCBI36
NG_012827.1:g.791628G>C
NG_012827.2:g.791628G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000418658.6:c.906G>C MANE Select	ENSP00000396010.1:p.Gly302=
ENST00000397461.5:c.906G>C	ENSP00000380602.1:p.Gly302=
ENST00000418658.5:c.906G>C	ENSP00000396010.1:p.Gly302=
ENST00000427331.5:c.906G>C	ENSP00000413642.1:p.Gly302=
ENST00000427741.5:c.*104G>C	ENSP00000396719.1:n.*104G>C
ENST00000430505.6:n.1103G>C
ENST00000438282.6:n.1342G>C
ENST00000473058.1:n.534G>C
NM_001206955.1:c.906G>C	NP_001193884.1:p.Gly302=
NM_175607.2:c.906G>C	NP_783200.1:p.Gly302=
XM_006713004.2:c.906G>C	XP_006713067.1:p.Gly302=
XM_011533425.1:c.906G>C	XP_011531727.1:p.Gly302=
XM_011533426.1:c.906G>C	XP_011531728.1:p.Gly302=
XM_011533427.1:c.906G>C	XP_011531729.1:p.Gly302=
XM_011533428.1:c.906G>C	XP_011531730.1:p.Gly302=
XM_011533429.1:c.906G>C	XP_011531731.1:p.Gly302=
XM_011533430.1:c.906G>C	XP_011531732.1:p.Gly302=
XM_011533431.1:c.873G>C	XP_011531733.1:p.Gly291=
NM_001350095.1:c.906G>C	NP_001337024.1:p.Gly302=
XM_006713004.4:c.906G>C	XP_006713067.1:p.Gly302=
XM_011533425.3:c.906G>C	XP_011531727.1:p.Gly302=
XM_011533427.2:c.906G>C	XP_011531729.1:p.Gly302=
XM_011533428.2:c.906G>C	XP_011531730.1:p.Gly302=
XM_011533429.2:c.906G>C	XP_011531731.1:p.Gly302=
XM_011533430.2:c.906G>C	XP_011531732.1:p.Gly302=
XM_011533431.2:c.873G>C	XP_011531733.1:p.Gly291=
XM_017005782.1:c.906G>C	XP_016861271.1:p.Gly302=
XM_017005783.1:c.906G>C	XP_016861272.1:p.Gly302=
XM_017005784.2:c.906G>C	XP_016861273.1:p.Gly302=
XM_017005785.1:c.906G>C	XP_016861274.1:p.Gly302=
XM_017005786.1:c.906G>C	XP_016861275.1:p.Gly302=
XM_017005787.1:c.906G>C	XP_016861276.1:p.Gly302=
NM_175607.3:c.906G>C MANE Select	NP_783200.1:p.Gly302=
NM_001206955.2:c.906G>C	NP_001193884.1:p.Gly302=
NM_001350095.2:c.906G>C	NP_001337024.1:p.Gly302=