Canonical Allele Identifier: CA2260596022

Gene: CNTNAP1 CCR10

Linked Data

• dbSNP Id: rs945039167

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682607G>C , CM000679.2:g.42682607G>C	GRCh38
NC_000017.10:g.40834625G>C , CM000679.1:g.40834625G>C	GRCh37
NC_000017.9:g.38088151G>C	NCBI36
NG_042091.1:g.4994G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-223G>C (CNTNAP1) MANE Select	ENSP00000264638.3:n.-223G>C
ENST00000591568.1:c.-643+1209C>G (CCR10)	ENSP00000467331.1:n.-643+1209C>G
ENST00000591765.1:c.-929C>G (CCR10)	ENSP00000468135.1:n.-929C>G
XM_017025238.1:c.-223G>C (CNTNAP1)	XP_016880727.1:n.-223G>C
XM_024451011.1:c.-223G>C (CNTNAP1)	XP_024306779.1:n.-223G>C
NM_003632.3:c.-223G>C (CNTNAP1) MANE Select	NP_003623.1:n.-223G>C