Canonical Allele Identifier: CA2576277899

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682827-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682827T>C , CM000679.2:g.42682827T>C	GRCh38
NC_000017.10:g.40834845T>C , CM000679.1:g.40834845T>C	GRCh37
NC_000017.9:g.38088371T>C	NCBI36
NG_042091.1:g.5214T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.-3T>C (CNTNAP1) MANE Select	ENSP00000264638.3:n.-3T>C
ENST00000264638.8:c.-3T>C (CNTNAP1)	ENSP00000264638.3:n.-3T>C
ENST00000591568.1:c.-643+989A>G (CCR10)	ENSP00000467331.1:n.-643+989A>G
ENST00000591662.1:c.-3T>C (CNTNAP1)	ENSP00000466571.1:n.-3T>C
ENST00000591765.1:c.-1149A>G (CCR10)	ENSP00000468135.1:n.-1149A>G
NM_003632.2:c.-3T>C (CNTNAP1)	NP_003623.1:n.-3T>C
XM_005257748.4:c.-1023T>C (CNTNAP1)	XP_005257805.1:n.-1023T>C
XM_017025238.1:c.-3T>C (CNTNAP1)	XP_016880727.1:n.-3T>C
XM_024451011.1:c.-3T>C (CNTNAP1)	XP_024306779.1:n.-3T>C
NM_003632.3:c.-3T>C (CNTNAP1) MANE Select	NP_003623.1:n.-3T>C