Canonical Allele Identifier: CA626068924

Gene: CNTNAP1 CCR10

Linked Data

• dbSNP Id: rs1488180401
• gnomAD v2: 17-40834561-T-C
• gnomAD v3: 17-42682543-T-C
• gnomAD v4: 17-42682543-T-C
• MyVariant Identifiers: chr17:g.40834561T>C (hg19) ; chr17:g.42682543T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682543T>C , CM000679.2:g.42682543T>C	GRCh38
NC_000017.10:g.40834561T>C , CM000679.1:g.40834561T>C	GRCh37
NC_000017.9:g.38088087T>C	NCBI36
NG_042091.1:g.4930T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-287T>C (CNTNAP1) MANE Select	ENSP00000264638.3:n.-287T>C
ENST00000591568.1:c.-643+1273A>G (CCR10)	ENSP00000467331.1:n.-643+1273A>G
ENST00000591765.1:c.-865A>G (CCR10)	ENSP00000468135.1:n.-865A>G
XM_017025238.1:c.-287T>C (CNTNAP1)	XP_016880727.1:n.-287T>C
XM_024451011.1:c.-287T>C (CNTNAP1)	XP_024306779.1:n.-287T>C
NM_003632.3:c.-287T>C (CNTNAP1) MANE Select	NP_003623.1:n.-287T>C