Canonical Allele Identifier: CA1750802235

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147485841T= , CM000669.2:g.147485841T=	GRCh38
NC_000007.13:g.147182933T= , CM000669.1:g.147182933T=	GRCh37
NC_000007.12:g.146813866T=	NCBI36
NG_007092.2:g.1374481T=
NG_007092.3:g.1374841T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.1671-94T= MANE Select	ENSP00000354778.3:n.1671-94T=
ENST00000636870.1:n.1533-94T=
ENST00000637694.1:n.1574-94T=
ENST00000637825.1:n.1154-94T=
ENST00000638117.1:n.1574-94T=
ENST00000361727.7:c.1671-94T=	ENSP00000354778.3:n.1671-94T=
NM_014141.5:c.1671-94T=	NP_054860.1:n.1671-94T=
XM_006715919.1:c.159-94T=	XP_006715982.1:n.159-94T=
XM_017011950.2:c.1671-94T=	XP_016867439.1:n.1671-94T=
NM_014141.6:c.1671-94T= MANE Select	NP_054860.1:n.1671-94T=