Canonical Allele Identifier: CA1750623620

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132180G= , CM000669.2:g.147132180G=	GRCh38
NC_000007.13:g.146829272G= , CM000669.1:g.146829272G=	GRCh37
NC_000007.12:g.146460205G=	NCBI36
NG_007092.2:g.1020820G=
NG_007092.3:g.1021180G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.1084-65G= MANE Select	ENSP00000354778.3:n.1084-65G=
ENST00000636561.1:n.987-65G=
ENST00000636870.1:n.946-65G=
ENST00000637150.1:n.1013-65G=
ENST00000637694.1:n.987-65G=
ENST00000637825.1:n.567-65G=
ENST00000638117.1:n.987-65G=
ENST00000361727.7:c.1084-65G=	ENSP00000354778.3:n.1084-65G=
NM_014141.5:c.1084-65G=	NP_054860.1:n.1084-65G=
XM_017011950.2:c.1084-65G=	XP_016867439.1:n.1084-65G=
NM_014141.6:c.1084-65G= MANE Select	NP_054860.1:n.1084-65G=