Canonical Allele Identifier: CA369924600

Gene: CNTNAP2

Linked Data

• MyVariant Identifiers: chr7:g.146829408G>C (hg19) ; chr7:g.147132316G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.147132316G>C , CM000669.2:g.147132316G>C	GRCh38
NC_000007.13:g.146829408G>C , CM000669.1:g.146829408G>C	GRCh37
NC_000007.12:g.146460341G>C	NCBI36
NG_007092.2:g.1020956G>C
NG_007092.3:g.1021316G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361727.8:c.1155G>C MANE Select	ENSP00000354778.3:p.Glu385Asp
ENST00000636561.1:n.1058G>C
ENST00000636870.1:n.1017G>C
ENST00000637150.1:n.1084G>C
ENST00000637694.1:n.1058G>C
ENST00000637825.1:n.638G>C
ENST00000638117.1:n.1058G>C
ENST00000361727.7:c.1155G>C	ENSP00000354778.3:p.Glu385Asp
NM_014141.5:c.1155G>C	NP_054860.1:p.Glu385Asp
XM_017011950.2:c.1155G>C	XP_016867439.1:p.Glu385Asp
NM_014141.6:c.1155G>C MANE Select	NP_054860.1:p.Glu385Asp