Canonical Allele Identifier: CA1750623948

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132353A= , CM000669.2:g.147132353A=	GRCh38
NC_000007.13:g.146829445A= , CM000669.1:g.146829445A=	GRCh37
NC_000007.12:g.146460378A=	NCBI36
NG_007092.2:g.1020993A=
NG_007092.3:g.1021353A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1192A= MANE Select	ENSP00000354778.3:p.Ser398=
ENST00000636561.1:n.1095A=
ENST00000636870.1:n.1054A=
ENST00000637150.1:n.1121A=
ENST00000637694.1:n.1095A=
ENST00000637825.1:n.675A=
ENST00000638117.1:n.1095A=
ENST00000361727.7:c.1192A=	ENSP00000354778.3:p.Ser398=
NM_014141.5:c.1192A=	NP_054860.1:p.Ser398=
XM_017011950.2:c.1192A=	XP_016867439.1:p.Ser398=
NM_014141.6:c.1192A= MANE Select	NP_054860.1:p.Ser398=