Canonical Allele Identifier: CA458577907
Gene: CNTNAP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.146829405G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132313G>T , CM000669.2:g.147132313G>T GRCh38
NC_000007.13:g.146829405G>T , CM000669.1:g.146829405G>T GRCh37
NC_000007.12:g.146460338G>T NCBI36
NG_007092.2:g.1020953G>T
NG_007092.3:g.1021313G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1152G>T MANE Select ENSP00000354778.3:p.Leu384=
ENST00000636561.1:n.1055G>T
ENST00000636870.1:n.1014G>T
ENST00000637150.1:n.1081G>T
ENST00000637694.1:n.1055G>T
ENST00000637825.1:n.635G>T
ENST00000638117.1:n.1055G>T
ENST00000361727.7:c.1152G>T ENSP00000354778.3:p.Leu384=
NM_014141.5:c.1152G>T NP_054860.1:p.Leu384=
XM_017011950.2:c.1152G>T XP_016867439.1:p.Leu384=
NM_014141.6:c.1152G>T MANE Select NP_054860.1:p.Leu384=