Canonical Allele Identifier: CA2238162569

Gene: CDH13

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83619245G= , CM000678.2:g.83619245G=	GRCh38
NC_000016.9:g.83652850G= , CM000678.1:g.83652850G=	GRCh37
NC_000016.8:g.82210351G=	NCBI36
NG_052819.1:g.997452G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000567109.6:c.1101+16651G= MANE Select	ENSP00000479395.1:n.1101+16651G=
ENST00000268613.14:c.1242+16651G=	ENSP00000268613.10:n.1242+16651G=
ENST00000428848.7:c.984+16651G=	ENSP00000394557.3:n.984+16651G=
ENST00000539548.6:c.*733+16651G=	ENSP00000442225.2:n.*733+16651G=
ENST00000566620.5:c.1065+16651G=	ENSP00000454435.3:n.1065+16651G=
ENST00000567109.5:c.1101+16651G=	ENSP00000479395.1:n.1101+16651G=
ENST00000622885.4:c.945+16651G=	ENSP00000483719.1:n.945+16651G=
NM_001220488.1:c.1242+16651G=	NP_001207417.1:n.1242+16651G=
NM_001220489.1:c.984+16651G=	NP_001207418.1:n.984+16651G=
NM_001220490.1:c.339+16651G=	NP_001207419.1:n.339+16651G=
NM_001257.4:c.1101+16651G=	NP_001248.1:n.1101+16651G=
XM_011522804.1:c.798+16651G=	XP_011521106.1:n.798+16651G=
XM_011522804.3:c.798+16651G=	XP_011521106.1:n.798+16651G=
NM_001257.5:c.1101+16651G= MANE Select	NP_001248.1:n.1101+16651G=
NM_001220488.2:c.1242+16651G=	NP_001207417.1:n.1242+16651G=
NM_001220489.2:c.984+16651G=	NP_001207418.1:n.984+16651G=
NM_001220490.2:c.339+16651G=	NP_001207419.1:n.339+16651G=