Canonical Allele Identifier: CA1750987879

Gene: CNTNAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147877725_147877730delinsGTTTTT , CM000669.2:g.147877725_147877730delinsGTTTTT	GRCh38
NC_000007.13:g.147574817_147574822delinsGTTTTT , CM000669.1:g.147574817_147574822delinsGTTTTT	GRCh37
NC_000007.12:g.147205750_147205755delinsGTTTTT	NCBI36
NG_007092.2:g.1766365_1766370delinsGTTTTT
NG_007092.3:g.1766725_1766730delinsGTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361727.8:c.2099-25840_2099-25835delinsGTTTTT MANE Select	ENSP00000354778.3:n.2099-25840_2099-25835delinsGTTTTT
ENST00000636870.1:n.1961-25840_1961-25835delinsGTTTTT
ENST00000637825.1:n.1582-25840_1582-25835delinsGTTTTT
ENST00000361727.7:c.2099-25840_2099-25835delinsGTTTTT	ENSP00000354778.3:n.2099-25840_2099-25835delinsGTTTTT
ENST00000455301.2:n.34-25840_34-25835delinsGTTTTT
ENST00000627772.2:n.272-25840_272-25835delinsGTTTTT
NM_014141.5:c.2099-25840_2099-25835delinsGTTTTT	NP_054860.1:n.2099-25840_2099-25835delinsGTTTTT
XM_006715919.1:c.587-25840_587-25835delinsGTTTTT	XP_006715982.1:n.587-25840_587-25835delinsGTTTTT
NM_014141.6:c.2099-25840_2099-25835delinsGTTTTT MANE Select	NP_054860.1:n.2099-25840_2099-25835delinsGTTTTT