Canonical Allele Identifier: CA2260596107

Gene: CNTNAP1 CCR10

Linked Data

• dbSNP Id: rs2052951246
• gnomAD v4: 17-42682748-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682748G>C , CM000679.2:g.42682748G>C	GRCh38
NC_000017.10:g.40834766G>C , CM000679.1:g.40834766G>C	GRCh37
NC_000017.9:g.38088292G>C	NCBI36
NG_042091.1:g.5135G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-82G>C (CNTNAP1) MANE Select	ENSP00000264638.3:n.-82G>C
ENST00000264638.8:c.-82G>C (CNTNAP1)	ENSP00000264638.3:n.-82G>C
ENST00000591568.1:c.-643+1068C>G (CCR10)	ENSP00000467331.1:n.-643+1068C>G
ENST00000591662.1:c.-82G>C (CNTNAP1)	ENSP00000466571.1:n.-82G>C
ENST00000591765.1:c.-1070C>G (CCR10)	ENSP00000468135.1:n.-1070C>G
NM_003632.2:c.-82G>C (CNTNAP1)	NP_003623.1:n.-82G>C
XM_005257748.4:c.-1102G>C (CNTNAP1)	XP_005257805.1:n.-1102G>C
XM_017025238.1:c.-82G>C (CNTNAP1)	XP_016880727.1:n.-82G>C
XM_024451011.1:c.-82G>C (CNTNAP1)	XP_024306779.1:n.-82G>C
NM_003632.3:c.-82G>C (CNTNAP1) MANE Select	NP_003623.1:n.-82G>C