Canonical Allele Identifier: CA623980163

Gene: CDH13

Linked Data

• dbSNP Id: rs1429519514
• gnomAD v2: 16-82817522-AAG-A
• gnomAD v3: 16-82783917-AAG-A
• gnomAD v4: 16-82783917-AAG-A
• MyVariant Identifiers: chr16:g.82817523_82817524del (hg19) ; chr16:g.82783918_82783919del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.82783919_82783920del , CM000678.2:g.82783919_82783920del	GRCh38
NC_000016.9:g.82817524_82817525del , CM000678.1:g.82817524_82817525del	GRCh37
NC_000016.8:g.81375025_81375026del	NCBI36
NG_052819.1:g.162126_162127del

Transcript Alleles

HGVS	Amino-acid change
ENST00000567109.6:c.46-74443_46-74442del MANE Select	ENSP00000479395.1:n.46-74443_46-74442del
ENST00000268613.14:c.187-74443_187-74442del	ENSP00000268613.10:n.187-74443_187-74442del
ENST00000428848.7:c.46-74443_46-74442del	ENSP00000394557.3:n.46-74443_46-74442del
ENST00000431540.7:c.46-74443_46-74442del	ENSP00000408632.3:n.46-74443_46-74442del
ENST00000539548.6:c.46-74443_46-74442del	ENSP00000442225.2:n.46-74443_46-74442del
ENST00000562601.5:c.*55-74443_*55-74442del	ENSP00000455781.1:n.*55-74443_*55-74442del
ENST00000565636.5:c.46-74443_46-74442del	ENSP00000456491.1:n.46-74443_46-74442del
ENST00000566333.1:n.168-74443_168-74442del
ENST00000567109.5:c.46-74443_46-74442del	ENSP00000479395.1:n.46-74443_46-74442del
ENST00000567445.1:c.46-74443_46-74442del	ENSP00000456297.1:n.46-74443_46-74442del
ENST00000568770.5:c.*45+64444_*45+64445del	ENSP00000457149.1:n.*45+64444_*45+64445del
ENST00000569144.5:c.46-74443_46-74442del	ENSP00000457914.1:n.46-74443_46-74442del
NM_001220488.1:c.187-74443_187-74442del	NP_001207417.1:n.187-74443_187-74442del
NM_001220489.1:c.46-74443_46-74442del	NP_001207418.1:n.46-74443_46-74442del
NM_001220490.1:c.-508-74443_-508-74442del	NP_001207419.1:n.-508-74443_-508-74442del
NM_001220491.1:c.46-74443_46-74442del	NP_001207420.1:n.46-74443_46-74442del
NM_001220492.1:c.46-74443_46-74442del	NP_001207421.1:n.46-74443_46-74442del
NM_001257.4:c.46-74443_46-74442del	NP_001248.1:n.46-74443_46-74442del
NR_110938.1:n.171+10430_171+10431del
XM_011522805.1:c.187-74443_187-74442del	XP_011521107.1:n.187-74443_187-74442del
XM_017022848.2:c.187-74443_187-74442del	XP_016878337.1:n.187-74443_187-74442del
XM_017022849.2:c.187-74443_187-74442del	XP_016878338.1:n.187-74443_187-74442del
NM_001257.5:c.46-74443_46-74442del MANE Select	NP_001248.1:n.46-74443_46-74442del
NM_001220488.2:c.187-74443_187-74442del	NP_001207417.1:n.187-74443_187-74442del
NM_001220489.2:c.46-74443_46-74442del	NP_001207418.1:n.46-74443_46-74442del
NM_001220490.2:c.-508-74443_-508-74442del	NP_001207419.1:n.-508-74443_-508-74442del
NM_001220491.2:c.46-74443_46-74442del	NP_001207420.1:n.46-74443_46-74442del
NM_001220492.2:c.46-74443_46-74442del	NP_001207421.1:n.46-74443_46-74442del