Canonical Allele Identifier: CA1750993399
Gene: CNTNAP2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147904511A= , CM000669.2:g.147904511A= GRCh38
NC_000007.13:g.147601603A= , CM000669.1:g.147601603A= GRCh37
NC_000007.12:g.147232536A= NCBI36
NG_007092.2:g.1793151A=
NG_007092.3:g.1793511A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.2255+790A= MANE Select ENSP00000354778.3:n.2255+790A=
ENST00000636870.1:n.2117+790A=
ENST00000637825.1:n.1738+790A=
ENST00000361727.7:c.2255+790A= ENSP00000354778.3:n.2255+790A=
ENST00000455301.2:n.190+790A=
ENST00000627772.2:n.428+790A=
NM_014141.5:c.2255+790A= NP_054860.1:n.2255+790A=
XM_006715919.1:c.743+790A= XP_006715982.1:n.743+790A=
NM_014141.6:c.2255+790A= MANE Select NP_054860.1:n.2255+790A=
Search 100 bp 5'
Search 100 bp 3'