Canonical Allele Identifier: CA1108379678
Gene: CNTNAP2 HGNC NCBI

Linked Data

dbSNP Id: rs1802425679

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.146778325A>T , CM000669.2:g.146778325A>T GRCh38
NC_000007.13:g.146475417A>T , CM000669.1:g.146475417A>T GRCh37
NC_000007.12:g.146106350A>T NCBI36
NG_007092.2:g.666965A>T
NG_007092.3:g.667325A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.208+3944A>T MANE Select ENSP00000354778.3:n.208+3944A>T
ENST00000636277.1:n.75+3944A>T
ENST00000636561.1:n.111+3944A>T
ENST00000636600.1:n.59-3884A>T
ENST00000637150.1:n.137+3944A>T
ENST00000637694.1:n.111+3944A>T
ENST00000638117.1:n.111+3944A>T
ENST00000361727.7:c.208+3944A>T ENSP00000354778.3:n.208+3944A>T
ENST00000625365.2:c.208+3944A>T ENSP00000485955.1:n.208+3944A>T
NM_014141.5:c.208+3944A>T NP_054860.1:n.208+3944A>T
XM_017011950.2:c.208+3944A>T XP_016867439.1:n.208+3944A>T
NM_014141.6:c.208+3944A>T MANE Select NP_054860.1:n.208+3944A>T