Canonical Allele Identifier: CA2031242420

Gene: CNTN1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40853940G= , CM000674.2:g.40853940G=	GRCh38
NC_000012.11:g.41247742G= , CM000674.1:g.41247742G=	GRCh37
NC_000012.10:g.39534009G=	NCBI36
NG_012058.2:g.166385G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001843.4:c.-76-54417G= MANE Select	NP_001834.2:n.-76-54417G=
ENST00000551295.7:c.-76-54417G= MANE Select	ENSP00000447006.1:n.-76-54417G=
NM_001256063.1:c.-76-54417G=	NP_001242992.1:n.-76-54417G=
NM_001256063.2:c.-76-54417G=	NP_001242992.1:n.-76-54417G=
NM_001256064.1:c.-77+25639G=	NP_001242993.1:n.-77+25639G=
NM_001256064.2:c.-77+25639G=	NP_001242993.1:n.-77+25639G=
NM_001843.3:c.-76-54417G=	NP_001834.2:n.-76-54417G=
ENST00000547702.5:c.-76-54417G=	ENSP00000448004.1:n.-76-54417G=
ENST00000547849.5:c.-77+25639G=	ENSP00000448653.1:n.-77+25639G=
ENST00000547849.6:c.-77+25639G=	ENSP00000448653.1:n.-77+25639G=
ENST00000548005.5:c.-76-54417G=	ENSP00000447862.1:n.-76-54417G=
ENST00000551295.6:c.-76-54417G=	ENSP00000447006.1:n.-76-54417G=
ENST00000551424.5:c.-236-42010G=	ENSP00000450412.1:n.-236-42010G=
ENST00000552248.5:c.-76-54417G=	ENSP00000447860.1:n.-76-54417G=
ENST00000552913.5:c.-237+25639G=	ENSP00000449706.1:n.-237+25639G=
XM_005268651.1:c.-77+25639G=	XP_005268708.1:n.-77+25639G=
XM_005268651.2:c.-77+25639G=	XP_005268708.1:n.-77+25639G=
XM_011537926.1:c.-76-54417G=	XP_011536228.1:n.-76-54417G=
XM_011537926.3:c.-76-54417G=	XP_011536228.1:n.-76-54417G=
XM_024448843.1:c.-76-54417G=	XP_024304611.1:n.-76-54417G=
XR_002957288.1:n.147-54417G=
XR_002957289.1:n.268-54417G=
XR_002957290.1:n.514+25639G=