Canonical Allele Identifier: CA1750623647

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132207_147132208delinsTC , CM000669.2:g.147132207_147132208delinsTC	GRCh38
NC_000007.13:g.146829299_146829300delinsTC , CM000669.1:g.146829299_146829300delinsTC	GRCh37
NC_000007.12:g.146460232_146460233delinsTC	NCBI36
NG_007092.2:g.1020847_1020848delinsTC
NG_007092.3:g.1021207_1021208delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.1084-38_1084-37delinsTC MANE Select	ENSP00000354778.3:n.1084-38_1084-37delins...
ENST00000636561.1:n.987-38_987-37delinsTC
ENST00000636870.1:n.946-38_946-37delinsTC
ENST00000637150.1:n.1013-38_1013-37delinsTC
ENST00000637694.1:n.987-38_987-37delinsTC
ENST00000637825.1:n.567-38_567-37delinsTC
ENST00000638117.1:n.987-38_987-37delinsTC
ENST00000361727.7:c.1084-38_1084-37delinsTC	ENSP00000354778.3:n.1084-38_1084-37delins...
NM_014141.5:c.1084-38_1084-37delinsTC	NP_054860.1:n.1084-38_1084-37delinsTC
XM_017011950.2:c.1084-38_1084-37delinsTC	XP_016867439.1:n.1084-38_1084-37delinsTC
NM_014141.6:c.1084-38_1084-37delinsTC MANE Select	NP_054860.1:n.1084-38_1084-37delinsTC