Canonical Allele Identifier: CA115521289
Gene: CDH12 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.21779045T>C , CM000667.2:g.21779045T>C GRCh38
NC_000005.9:g.21779154T>C , CM000667.1:g.21779154T>C GRCh37
NC_000005.8:g.21814911T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000382254.6:c.1393+4313A>G MANE Select ENSP00000371689.1:n.1393+4313A>G
ENST00000382254.5:c.1393+4313A>G ENSP00000371689.1:n.1393+4313A>G
ENST00000504376.6:c.1393+4313A>G ENSP00000423577.1:n.1393+4313A>G
ENST00000517378.1:n.1851+4313A>G
ENST00000521384.5:n.1130+4313A>G
ENST00000522262.1:c.1273+4313A>G ENSP00000428786.1:n.1273+4313A>G
ENST00000619694.4:c.1393+4313A>G ENSP00000480493.1:n.1393+4313A>G
NM_004061.3:c.1393+4313A>G NP_004052.2:n.1393+4313A>G
XM_011513927.1:c.1393+4313A>G XP_011512229.1:n.1393+4313A>G
XR_925847.1:n.691-23129T>C
NM_001317227.1:c.1393+4313A>G NP_001304156.1:n.1393+4313A>G
NM_001317228.1:c.1273+4313A>G NP_001304157.1:n.1273+4313A>G
NM_001364104.1:c.1393+4313A>G NP_001351033.1:n.1393+4313A>G
NM_001364105.1:c.1393+4313A>G NP_001351034.1:n.1393+4313A>G
NM_001364106.1:c.1393+4313A>G NP_001351035.1:n.1393+4313A>G
NM_001364107.1:c.1393+4313A>G NP_001351036.1:n.1393+4313A>G
NM_001364108.1:c.1393+4313A>G NP_001351037.1:n.1393+4313A>G
NM_001364109.1:c.721+4313A>G NP_001351038.1:n.721+4313A>G
NM_004061.4:c.1393+4313A>G NP_004052.2:n.1393+4313A>G
NM_001364104.2:c.1393+4313A>G NP_001351033.1:n.1393+4313A>G
NM_001364105.2:c.1393+4313A>G NP_001351034.1:n.1393+4313A>G
NM_001364106.2:c.1393+4313A>G NP_001351035.1:n.1393+4313A>G
NM_004061.5:c.1393+4313A>G MANE Select NP_004052.2:n.1393+4313A>G
NM_001317227.2:c.1393+4313A>G NP_001304156.1:n.1393+4313A>G
NM_001364107.2:c.1393+4313A>G NP_001351036.1:n.1393+4313A>G
NM_001364108.2:c.1393+4313A>G NP_001351037.1:n.1393+4313A>G
NM_001364109.2:c.721+4313A>G NP_001351038.1:n.721+4313A>G
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