Canonical Allele Identifier: CA623810486

Gene: CDH13

Linked Data

• dbSNP Id: rs1195530120
• gnomAD v2: 16-83709695-G-A
• gnomAD v3: 16-83676090-G-A
• gnomAD v4: 16-83676090-G-A
• MyVariant Identifiers: chr16:g.83709695G>A (hg19) ; chr16:g.83676090G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83676090G>A , CM000678.2:g.83676090G>A	GRCh38
NC_000016.9:g.83709695G>A , CM000678.1:g.83709695G>A	GRCh37
NC_000016.8:g.82267196G>A	NCBI36
NG_052819.1:g.1054297G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567109.6:c.1285-2118G>A MANE Select	ENSP00000479395.1:n.1285-2118G>A
ENST00000268613.14:c.1426-2118G>A	ENSP00000268613.10:n.1426-2118G>A
ENST00000428848.7:c.1168-2118G>A	ENSP00000394557.3:n.1168-2118G>A
ENST00000539548.6:c.*917-2118G>A	ENSP00000442225.2:n.*917-2118G>A
ENST00000566620.5:c.1249-2118G>A	ENSP00000454435.3:n.1249-2118G>A
ENST00000567109.5:c.1285-2118G>A	ENSP00000479395.1:n.1285-2118G>A
ENST00000615627.1:c.205-2118G>A	ENSP00000482651.1:n.205-2118G>A
ENST00000622885.4:c.1129-2118G>A	ENSP00000483719.1:n.1129-2118G>A
NM_001220488.1:c.1426-2118G>A	NP_001207417.1:n.1426-2118G>A
NM_001220489.1:c.1168-2118G>A	NP_001207418.1:n.1168-2118G>A
NM_001220490.1:c.523-2118G>A	NP_001207419.1:n.523-2118G>A
NM_001257.4:c.1285-2118G>A	NP_001248.1:n.1285-2118G>A
XM_011522804.1:c.982-2118G>A	XP_011521106.1:n.982-2118G>A
XM_011522804.3:c.982-2118G>A	XP_011521106.1:n.982-2118G>A
XR_001752385.2:n.6466-8499C>T
NM_001257.5:c.1285-2118G>A MANE Select	NP_001248.1:n.1285-2118G>A
NM_001220488.2:c.1426-2118G>A	NP_001207417.1:n.1426-2118G>A
NM_001220489.2:c.1168-2118G>A	NP_001207418.1:n.1168-2118G>A
NM_001220490.2:c.523-2118G>A	NP_001207419.1:n.523-2118G>A