Canonical Allele Identifier: CA285844580
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs11150556
MyVariant Identifiers: chr16:g.83236936T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83236936T>G , CM000678.2:g.83236936T>G GRCh38
NC_000016.9:g.83270541T>G , CM000678.1:g.83270541T>G GRCh37
NC_000016.8:g.81828042T>G NCBI36
NG_052819.1:g.615143T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000567109.6:c.636+19439T>G MANE Select ENSP00000479395.1:p.=
ENST00000268613.14:c.777+19439T>G ENSP00000268613.10:p.=
ENST00000428848.7:c.519+19439T>G ENSP00000394557.3:p.=
ENST00000539548.6:c.*268+19439T>G ENSP00000442225.2:p.=
ENST00000566620.5:n.600+19439T>G ENSP00000454435.3:p.=
ENST00000567109.5:c.636+19439T>G ENSP00000479395.1:p.=
ENST00000569454.1:n.553+19439T>G
ENST00000622885.4:n.480+19439T>G ENSP00000483719.1:p.=
NM_001220488.1:c.777+19439T>G NP_001207417.1:p.=
NM_001220489.1:c.519+19439T>G NP_001207418.1:p.=
NM_001220490.1:c.-127+19439T>G NP_001207419.1:p.=
NM_001257.4:c.636+19439T>G NP_001248.1:p.=
XM_011522804.1:c.333+19439T>G XP_011521106.1:p.=
XM_011522805.1:c.777+19439T>G XP_011521107.1:p.=
XM_011522804.3:c.333+19439T>G XP_011521106.1:p.=
XM_017022848.2:c.777+19439T>G XP_016878337.1:p.=
NM_001257.5:c.636+19439T>G MANE Select NP_001248.1:p.=
NM_001220488.2:c.777+19439T>G NP_001207417.1:p.=
NM_001220489.2:c.519+19439T>G NP_001207418.1:p.=
NM_001220490.2:c.-127+19439T>G NP_001207419.1:p.=