Canonical Allele Identifier: CA285366419

Gene: CDH13

Linked Data

• dbSNP Id: rs929023425
• MyVariant Identifiers: chr16:g.83709572G>C (hg19) ; chr16:g.83675967G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83675967G>C , CM000678.2:g.83675967G>C	GRCh38
NC_000016.9:g.83709572G>C , CM000678.1:g.83709572G>C	GRCh37
NC_000016.8:g.82267073G>C	NCBI36
NG_052819.1:g.1054174G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000567109.6:c.1285-2241G>C MANE Select	ENSP00000479395.1:n.1285-2241G>C
ENST00000268613.14:c.1426-2241G>C	ENSP00000268613.10:n.1426-2241G>C
ENST00000428848.7:c.1168-2241G>C	ENSP00000394557.3:n.1168-2241G>C
ENST00000539548.6:c.*917-2241G>C	ENSP00000442225.2:n.*917-2241G>C
ENST00000566620.5:c.1249-2241G>C	ENSP00000454435.3:n.1249-2241G>C
ENST00000567109.5:c.1285-2241G>C	ENSP00000479395.1:n.1285-2241G>C
ENST00000615627.1:c.205-2241G>C	ENSP00000482651.1:n.205-2241G>C
ENST00000622885.4:c.1129-2241G>C	ENSP00000483719.1:n.1129-2241G>C
NM_001220488.1:c.1426-2241G>C	NP_001207417.1:n.1426-2241G>C
NM_001220489.1:c.1168-2241G>C	NP_001207418.1:n.1168-2241G>C
NM_001220490.1:c.523-2241G>C	NP_001207419.1:n.523-2241G>C
NM_001257.4:c.1285-2241G>C	NP_001248.1:n.1285-2241G>C
XM_011522804.1:c.982-2241G>C	XP_011521106.1:n.982-2241G>C
XM_011522804.3:c.982-2241G>C	XP_011521106.1:n.982-2241G>C
XR_001752385.2:n.6466-8376C>G
NM_001257.5:c.1285-2241G>C MANE Select	NP_001248.1:n.1285-2241G>C
NM_001220488.2:c.1426-2241G>C	NP_001207417.1:n.1426-2241G>C
NM_001220489.2:c.1168-2241G>C	NP_001207418.1:n.1168-2241G>C
NM_001220490.2:c.523-2241G>C	NP_001207419.1:n.523-2241G>C