Canonical Allele Identifier: CA772112079

Gene: CNTNAP1 CCR10

Linked Data

• dbSNP Id: rs1191923604
• MyVariant Identifiers: chr17:g.40834786A>C (hg19) ; chr17:g.42682768A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682768A>C , CM000679.2:g.42682768A>C	GRCh38
NC_000017.10:g.40834786A>C , CM000679.1:g.40834786A>C	GRCh37
NC_000017.9:g.38088312A>C	NCBI36
NG_042091.1:g.5155A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-62A>C (CNTNAP1) MANE Select	ENSP00000264638.3:n.-62A>C
ENST00000264638.8:c.-62A>C (CNTNAP1)	ENSP00000264638.3:n.-62A>C
ENST00000591568.1:c.-643+1048T>G (CCR10)	ENSP00000467331.1:n.-643+1048T>G
ENST00000591662.1:c.-62A>C (CNTNAP1)	ENSP00000466571.1:n.-62A>C
ENST00000591765.1:c.-1090T>G (CCR10)	ENSP00000468135.1:n.-1090T>G
NM_003632.2:c.-62A>C (CNTNAP1)	NP_003623.1:n.-62A>C
XM_005257748.4:c.-1082A>C (CNTNAP1)	XP_005257805.1:n.-1082A>C
XM_017025238.1:c.-62A>C (CNTNAP1)	XP_016880727.1:n.-62A>C
XM_024451011.1:c.-62A>C (CNTNAP1)	XP_024306779.1:n.-62A>C
NM_003632.3:c.-62A>C (CNTNAP1) MANE Select	NP_003623.1:n.-62A>C