Canonical Allele Identifier: CA1750623912

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132334C= , CM000669.2:g.147132334C=	GRCh38
NC_000007.13:g.146829426C= , CM000669.1:g.146829426C=	GRCh37
NC_000007.12:g.146460359C=	NCBI36
NG_007092.2:g.1020974C=
NG_007092.3:g.1021334C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.1173C= MANE Select	ENSP00000354778.3:p.Asn391=
ENST00000636561.1:n.1076C=
ENST00000636870.1:n.1035C=
ENST00000637150.1:n.1102C=
ENST00000637694.1:n.1076C=
ENST00000637825.1:n.656C=
ENST00000638117.1:n.1076C=
ENST00000361727.7:c.1173C=	ENSP00000354778.3:p.Asn391=
NM_014141.5:c.1173C=	NP_054860.1:p.Asn391=
XM_017011950.2:c.1173C=	XP_016867439.1:p.Asn391=
NM_014141.6:c.1173C= MANE Select	NP_054860.1:p.Asn391=