Canonical Allele Identifier: CA285892840

Gene: CDH13

Linked Data

• dbSNP Id: rs1044919823
• MyVariant Identifiers: chr16:g.83527886T>C (hg19) ; chr16:g.83494281T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83494281T>C , CM000678.2:g.83494281T>C	GRCh38
NC_000016.9:g.83527886T>C , CM000678.1:g.83527886T>C	GRCh37
NC_000016.8:g.82085387T>C	NCBI36
NG_052819.1:g.872488T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567109.6:c.960+7626T>C MANE Select	ENSP00000479395.1:n.960+7626T>C
ENST00000268613.14:c.1101+7626T>C	ENSP00000268613.10:n.1101+7626T>C
ENST00000428848.7:c.843+7626T>C	ENSP00000394557.3:n.843+7626T>C
ENST00000539548.6:c.*592+7626T>C	ENSP00000442225.2:n.*592+7626T>C
ENST00000566620.5:c.924+7626T>C	ENSP00000454435.3:n.924+7626T>C
ENST00000567109.5:c.960+7626T>C	ENSP00000479395.1:n.960+7626T>C
ENST00000622885.4:c.804+7626T>C	ENSP00000483719.1:n.804+7626T>C
NM_001220488.1:c.1101+7626T>C	NP_001207417.1:n.1101+7626T>C
NM_001220489.1:c.843+7626T>C	NP_001207418.1:n.843+7626T>C
NM_001220490.1:c.198+7626T>C	NP_001207419.1:n.198+7626T>C
NM_001257.4:c.960+7626T>C	NP_001248.1:n.960+7626T>C
XM_011522804.1:c.657+7626T>C	XP_011521106.1:n.657+7626T>C
XM_011522805.1:c.1101+7626T>C	XP_011521107.1:n.1101+7626T>C
XM_011522804.3:c.657+7626T>C	XP_011521106.1:n.657+7626T>C
XM_017022848.2:c.1101+7626T>C	XP_016878337.1:n.1101+7626T>C
NM_001257.5:c.960+7626T>C MANE Select	NP_001248.1:n.960+7626T>C
NM_001220488.2:c.1101+7626T>C	NP_001207417.1:n.1101+7626T>C
NM_001220489.2:c.843+7626T>C	NP_001207418.1:n.843+7626T>C
NM_001220490.2:c.198+7626T>C	NP_001207419.1:n.198+7626T>C