Canonical Allele Identifier: CA1750443651
Gene: CNTNAP2 HGNC NCBI

Linked Data

dbSNP Id: rs1410840516

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.146792326A>T , CM000669.2:g.146792326A>T GRCh38
NC_000007.13:g.146489418A>T , CM000669.1:g.146489418A>T GRCh37
NC_000007.12:g.146120351A>T NCBI36
NG_007092.2:g.680966A>T
NG_007092.3:g.681326A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.208+17945A>T MANE Select ENSP00000354778.3:n.208+17945A>T
ENST00000636561.1:n.111+17945A>T
ENST00000637150.1:n.137+17945A>T
ENST00000637694.1:n.111+17945A>T
ENST00000638117.1:n.111+17945A>T
ENST00000361727.7:c.208+17945A>T ENSP00000354778.3:n.208+17945A>T
ENST00000625365.2:c.208+17945A>T ENSP00000485955.1:n.208+17945A>T
NM_014141.5:c.208+17945A>T NP_054860.1:n.208+17945A>T
XM_017011950.2:c.208+17945A>T XP_016867439.1:n.208+17945A>T
NM_014141.6:c.208+17945A>T MANE Select NP_054860.1:n.208+17945A>T