Canonical Allele Identifier: CA14288499

Gene: CDH13

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83605730G>A , CM000678.2:g.83605730G>A	GRCh38
NC_000016.9:g.83639335G>A , CM000678.1:g.83639335G>A	GRCh37
NC_000016.8:g.82196836G>A	NCBI36
NG_052819.1:g.983937G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567109.6:c.1101+3136G>A MANE Select	ENSP00000479395.1:n.1101+3136G>A
ENST00000268613.14:c.1242+3136G>A	ENSP00000268613.10:n.1242+3136G>A
ENST00000428848.7:c.984+3136G>A	ENSP00000394557.3:n.984+3136G>A
ENST00000539548.6:c.*733+3136G>A	ENSP00000442225.2:n.*733+3136G>A
ENST00000566620.5:c.1065+3136G>A	ENSP00000454435.3:n.1065+3136G>A
ENST00000567109.5:c.1101+3136G>A	ENSP00000479395.1:n.1101+3136G>A
ENST00000622885.4:c.945+3136G>A	ENSP00000483719.1:n.945+3136G>A
NM_001220488.1:c.1242+3136G>A	NP_001207417.1:n.1242+3136G>A
NM_001220489.1:c.984+3136G>A	NP_001207418.1:n.984+3136G>A
NM_001220490.1:c.339+3136G>A	NP_001207419.1:n.339+3136G>A
NM_001257.4:c.1101+3136G>A	NP_001248.1:n.1101+3136G>A
XM_011522804.1:c.798+3136G>A	XP_011521106.1:n.798+3136G>A
XM_011522805.1:c.1242+3136G>A	XP_011521107.1:n.1242+3136G>A
XM_011522804.3:c.798+3136G>A	XP_011521106.1:n.798+3136G>A
NM_001257.5:c.1101+3136G>A MANE Select	NP_001248.1:n.1101+3136G>A
NM_001220488.2:c.1242+3136G>A	NP_001207417.1:n.1242+3136G>A
NM_001220489.2:c.984+3136G>A	NP_001207418.1:n.984+3136G>A
NM_001220490.2:c.339+3136G>A	NP_001207419.1:n.339+3136G>A