Canonical Allele Identifier: CA1751124856

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.148147442G= , CM000669.2:g.148147442G=	GRCh38
NC_000007.13:g.147844534G= , CM000669.1:g.147844534G=	GRCh37
NC_000007.12:g.147475467G=	NCBI36
NG_007092.2:g.2036082G=
NG_007092.3:g.2036442G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.2555-49G= MANE Select	ENSP00000354778.3:n.2555-49G=
ENST00000636870.1:n.2417-49G=
ENST00000637020.1:n.373-49G=
ENST00000361727.7:c.2555-49G=	ENSP00000354778.3:n.2555-49G=
ENST00000627772.2:n.728-49G=
ENST00000628930.2:c.-269-49G=	ENSP00000487516.1:n.-269-49G=
ENST00000631199.2:n.284-49G=
NM_014141.5:c.2555-49G=	NP_054860.1:n.2555-49G=
XM_006715919.1:c.1043-49G=	XP_006715982.1:n.1043-49G=
XR_928095.1:n.214+7735C=
NM_014141.6:c.2555-49G= MANE Select	NP_054860.1:n.2555-49G=