Canonical Allele Identifier: CA2637988772

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682690-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682690A>G , CM000679.2:g.42682690A>G	GRCh38
NC_000017.10:g.40834708A>G , CM000679.1:g.40834708A>G	GRCh37
NC_000017.9:g.38088234A>G	NCBI36
NG_042091.1:g.5077A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-140A>G (CNTNAP1) MANE Select	ENSP00000264638.3:n.-140A>G
ENST00000264638.8:c.-140A>G (CNTNAP1)	ENSP00000264638.3:n.-140A>G
ENST00000591568.1:c.-643+1126T>C (CCR10)	ENSP00000467331.1:n.-643+1126T>C
ENST00000591765.1:c.-1012T>C (CCR10)	ENSP00000468135.1:n.-1012T>C
NM_003632.2:c.-140A>G (CNTNAP1)	NP_003623.1:n.-140A>G
XM_005257748.4:c.-1160A>G (CNTNAP1)	XP_005257805.1:n.-1160A>G
XM_017025238.1:c.-140A>G (CNTNAP1)	XP_016880727.1:n.-140A>G
XM_024451011.1:c.-140A>G (CNTNAP1)	XP_024306779.1:n.-140A>G
NM_003632.3:c.-140A>G (CNTNAP1) MANE Select	NP_003623.1:n.-140A>G