Canonical Allele Identifier: CA724967202

Gene: CDH13

Linked Data

• dbSNP Id: rs1310392398
• gnomAD v3: 16-83236960-A-AT
• gnomAD v4: 16-83236960-A-AT
• MyVariant Identifiers: chr16:g.83270565_83270566insT (hg19) ; chr16:g.83236960_83236961insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83236964dup , CM000678.2:g.83236964dup	GRCh38
NC_000016.9:g.83270569dup , CM000678.1:g.83270569dup	GRCh37
NC_000016.8:g.81828070dup	NCBI36
NG_052819.1:g.615171dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567109.6:c.636+19467dup MANE Select	ENSP00000479395.1:n.636+19467dup
ENST00000268613.14:c.777+19467dup	ENSP00000268613.10:n.777+19467dup
ENST00000428848.7:c.519+19467dup	ENSP00000394557.3:n.519+19467dup
ENST00000539548.6:c.*268+19467dup	ENSP00000442225.2:n.*268+19467dup
ENST00000566620.5:c.600+19467dup	ENSP00000454435.3:n.600+19467dup
ENST00000567109.5:c.636+19467dup	ENSP00000479395.1:n.636+19467dup
ENST00000569454.1:n.553+19467dup
ENST00000622885.4:c.480+19467dup	ENSP00000483719.1:n.480+19467dup
NM_001220488.1:c.777+19467dup	NP_001207417.1:n.777+19467dup
NM_001220489.1:c.519+19467dup	NP_001207418.1:n.519+19467dup
NM_001220490.1:c.-127+19467dup	NP_001207419.1:n.-127+19467dup
NM_001257.4:c.636+19467dup	NP_001248.1:n.636+19467dup
XM_011522804.1:c.333+19467dup	XP_011521106.1:n.333+19467dup
XM_011522805.1:c.777+19467dup	XP_011521107.1:n.777+19467dup
XM_011522804.3:c.333+19467dup	XP_011521106.1:n.333+19467dup
XM_017022848.2:c.777+19467dup	XP_016878337.1:n.777+19467dup
NM_001257.5:c.636+19467dup MANE Select	NP_001248.1:n.636+19467dup
NM_001220488.2:c.777+19467dup	NP_001207417.1:n.777+19467dup
NM_001220489.2:c.519+19467dup	NP_001207418.1:n.519+19467dup
NM_001220490.2:c.-127+19467dup	NP_001207419.1:n.-127+19467dup