Canonical Allele Identifier: CA2637988774

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682691-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682691G>A , CM000679.2:g.42682691G>A	GRCh38
NC_000017.10:g.40834709G>A , CM000679.1:g.40834709G>A	GRCh37
NC_000017.9:g.38088235G>A	NCBI36
NG_042091.1:g.5078G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-139G>A (CNTNAP1) MANE Select	ENSP00000264638.3:n.-139G>A
ENST00000264638.8:c.-139G>A (CNTNAP1)	ENSP00000264638.3:n.-139G>A
ENST00000591568.1:c.-643+1125C>T (CCR10)	ENSP00000467331.1:n.-643+1125C>T
ENST00000591765.1:c.-1013C>T (CCR10)	ENSP00000468135.1:n.-1013C>T
NM_003632.2:c.-139G>A (CNTNAP1)	NP_003623.1:n.-139G>A
XM_005257748.4:c.-1159G>A (CNTNAP1)	XP_005257805.1:n.-1159G>A
XM_017025238.1:c.-139G>A (CNTNAP1)	XP_016880727.1:n.-139G>A
XM_024451011.1:c.-139G>A (CNTNAP1)	XP_024306779.1:n.-139G>A
NM_003632.3:c.-139G>A (CNTNAP1) MANE Select	NP_003623.1:n.-139G>A