Canonical Allele Identifier: CA290789029

Gene: CNTNAP1 CCR10

Linked Data

• dbSNP Id: rs1010539667
• gnomAD v3: 17-42682622-A-G
• gnomAD v4: 17-42682622-A-G
• MyVariant Identifiers: chr17:g.40834640A>G (hg19) ; chr17:g.42682622A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682622A>G , CM000679.2:g.42682622A>G	GRCh38
NC_000017.10:g.40834640A>G , CM000679.1:g.40834640A>G	GRCh37
NC_000017.9:g.38088166A>G	NCBI36
NG_042091.1:g.5009A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-208A>G (CNTNAP1) MANE Select	ENSP00000264638.3:n.-208A>G
ENST00000264638.8:c.-208A>G (CNTNAP1)	ENSP00000264638.3:n.-208A>G
ENST00000591568.1:c.-643+1194T>C (CCR10)	ENSP00000467331.1:n.-643+1194T>C
ENST00000591765.1:c.-944T>C (CCR10)	ENSP00000468135.1:n.-944T>C
NM_003632.2:c.-208A>G (CNTNAP1)	NP_003623.1:n.-208A>G
XM_017025238.1:c.-208A>G (CNTNAP1)	XP_016880727.1:n.-208A>G
XM_024451011.1:c.-208A>G (CNTNAP1)	XP_024306779.1:n.-208A>G
NM_003632.3:c.-208A>G (CNTNAP1) MANE Select	NP_003623.1:n.-208A>G