Canonical Allele Identifier: CA369924898
Gene: CNTNAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132456G>A , CM000669.2:g.147132456G>A GRCh38
NC_000007.13:g.146829548G>A , CM000669.1:g.146829548G>A GRCh37
NC_000007.12:g.146460481G>A NCBI36
NG_007092.2:g.1021096G>A
NG_007092.3:g.1021456G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.1295G>A MANE Select ENSP00000354778.3:p.Gly432Asp
ENST00000636561.1:n.1198G>A
ENST00000636870.1:n.1157G>A
ENST00000637150.1:n.1224G>A
ENST00000637694.1:n.1198G>A
ENST00000637825.1:n.778G>A
ENST00000638117.1:n.1198G>A
ENST00000361727.7:c.1295G>A ENSP00000354778.3:p.Gly432Asp
NM_014141.5:c.1295G>A NP_054860.1:p.Gly432Asp
XM_017011950.2:c.1295G>A XP_016867439.1:p.Gly432Asp
NM_014141.6:c.1295G>A MANE Select NP_054860.1:p.Gly432Asp