Canonical Allele Identifier: CA2637988811

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682711-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682711T>G , CM000679.2:g.42682711T>G	GRCh38
NC_000017.10:g.40834729T>G , CM000679.1:g.40834729T>G	GRCh37
NC_000017.9:g.38088255T>G	NCBI36
NG_042091.1:g.5098T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-119T>G (CNTNAP1) MANE Select	ENSP00000264638.3:n.-119T>G
ENST00000264638.8:c.-119T>G (CNTNAP1)	ENSP00000264638.3:n.-119T>G
ENST00000591568.1:c.-643+1105A>C (CCR10)	ENSP00000467331.1:n.-643+1105A>C
ENST00000591662.1:c.-119T>G (CNTNAP1)	ENSP00000466571.1:n.-119T>G
ENST00000591765.1:c.-1033A>C (CCR10)	ENSP00000468135.1:n.-1033A>C
NM_003632.2:c.-119T>G (CNTNAP1)	NP_003623.1:n.-119T>G
XM_005257748.4:c.-1139T>G (CNTNAP1)	XP_005257805.1:n.-1139T>G
XM_017025238.1:c.-119T>G (CNTNAP1)	XP_016880727.1:n.-119T>G
XM_024451011.1:c.-119T>G (CNTNAP1)	XP_024306779.1:n.-119T>G
NM_003632.3:c.-119T>G (CNTNAP1) MANE Select	NP_003623.1:n.-119T>G