Canonical Allele Identifier: CA772112023

Gene: CNTNAP1 CCR10

Linked Data

• dbSNP Id: rs1200796744
• MyVariant Identifiers: chr17:g.40834666G>A (hg19) ; chr17:g.42682648G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682648G>A , CM000679.2:g.42682648G>A	GRCh38
NC_000017.10:g.40834666G>A , CM000679.1:g.40834666G>A	GRCh37
NC_000017.9:g.38088192G>A	NCBI36
NG_042091.1:g.5035G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-182G>A (CNTNAP1) MANE Select	ENSP00000264638.3:n.-182G>A
ENST00000264638.8:c.-182G>A (CNTNAP1)	ENSP00000264638.3:n.-182G>A
ENST00000591568.1:c.-643+1168C>T (CCR10)	ENSP00000467331.1:n.-643+1168C>T
ENST00000591765.1:c.-970C>T (CCR10)	ENSP00000468135.1:n.-970C>T
NM_003632.2:c.-182G>A (CNTNAP1)	NP_003623.1:n.-182G>A
XM_005257748.4:c.-1202G>A (CNTNAP1)	XP_005257805.1:n.-1202G>A
XM_017025238.1:c.-182G>A (CNTNAP1)	XP_016880727.1:n.-182G>A
XM_024451011.1:c.-182G>A (CNTNAP1)	XP_024306779.1:n.-182G>A
NM_003632.3:c.-182G>A (CNTNAP1) MANE Select	NP_003623.1:n.-182G>A