Canonical Allele Identifier: CA500089365

Gene: CNTNAP1 CCR10

Linked Data

• gnomAD v4: 17-42682868-G-A
• MyVariant Identifiers: chr17:g.40834886G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42682868G>A , CM000679.2:g.42682868G>A	GRCh38
NC_000017.10:g.40834886G>A , CM000679.1:g.40834886G>A	GRCh37
NC_000017.9:g.38088412G>A	NCBI36
NG_042091.1:g.5255G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264638.9:c.39G>A (CNTNAP1) MANE Select	ENSP00000264638.3:p.Ala13=
ENST00000264638.8:c.39G>A (CNTNAP1)	ENSP00000264638.3:p.Ala13=
ENST00000591568.1:c.-643+948C>T (CCR10)	ENSP00000467331.1:n.-643+948C>T
ENST00000591662.1:c.39G>A (CNTNAP1)	ENSP00000466571.1:p.Ala13=
ENST00000591765.1:c.-1190C>T (CCR10)	ENSP00000468135.1:n.-1190C>T
NM_003632.2:c.39G>A (CNTNAP1)	NP_003623.1:p.Ala13=
XM_005257748.4:c.-982G>A (CNTNAP1)	XP_005257805.1:n.-982G>A
XM_017025238.1:c.39G>A (CNTNAP1)	XP_016880727.1:p.Ala13=
XM_024451011.1:c.39G>A (CNTNAP1)	XP_024306779.1:p.Ala13=
NM_003632.3:c.39G>A (CNTNAP1) MANE Select	NP_003623.1:p.Ala13=