Canonical Allele Identifier: CA1750993541
Gene: CNTNAP2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147904684T= , CM000669.2:g.147904684T= GRCh38
NC_000007.13:g.147601776T= , CM000669.1:g.147601776T= GRCh37
NC_000007.12:g.147232709T= NCBI36
NG_007092.2:g.1793324T=
NG_007092.3:g.1793684T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.2255+963T= MANE Select ENSP00000354778.3:n.2255+963T=
ENST00000636870.1:n.2117+963T=
ENST00000637825.1:n.1738+963T=
ENST00000361727.7:c.2255+963T= ENSP00000354778.3:n.2255+963T=
ENST00000455301.2:n.190+963T=
ENST00000627772.2:n.428+963T=
NM_014141.5:c.2255+963T= NP_054860.1:n.2255+963T=
XM_006715919.1:c.743+963T= XP_006715982.1:n.743+963T=
NM_014141.6:c.2255+963T= MANE Select NP_054860.1:n.2255+963T=
Search 100 bp 5'
Search 100 bp 3'