Canonical Allele Identifier: CA367534752

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50476636G>C , CM000669.2:g.50476636G>C GRCh38
NC_000007.13:g.50544334G>C , CM000669.1:g.50544334G>C GRCh37
NC_000007.12:g.50511828G>C NCBI36
NG_008742.1:g.93821C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000444124.7:c.1029C>G (DDC) MANE Select ENSP00000403644.2:p.Ile343Met
ENST00000357936.9:c.1029C>G (DDC) ENSP00000350616.5:p.Ile343Met
ENST00000426377.5:c.795C>G (DDC) ENSP00000395069.1:p.Ile265Met
ENST00000430300.5:c.671C>G (DDC)
ENST00000431062.5:c.750C>G (DDC) ENSP00000399184.1:p.Ile250Met
ENST00000444124.6:c.1029C>G (DDC) ENSP00000403644.2:p.Ile343Met
ENST00000444733.5:c.*130C>G (DDC) ENSP00000393724.1:n.*130C>G
ENST00000494914.1:n.185C>G (DDC)
ENST00000613602.3:c.-10-29339C>G (FIGNL1) ENSP00000481751.1:n.-10-29339C>G
ENST00000615193.4:c.750C>G (DDC) ENSP00000484104.1:p.Ile250Met
ENST00000617822.4:c.885C>G (DDC) ENSP00000478385.1:p.Ile295Met
ENST00000622873.4:c.915C>G (DDC) ENSP00000479110.1:p.Ile305Met
NM_000790.3:c.1029C>G (DDC) NP_000781.1:p.Ile343Met
NM_001082971.1:c.1029C>G (DDC) NP_001076440.1:p.Ile343Met
NM_001242886.1:c.915C>G (DDC) NP_001229815.1:p.Ile305Met
NM_001242887.1:c.885C>G (DDC) NP_001229816.1:p.Ile295Met
NM_001242888.1:c.795C>G (DDC) NP_001229817.1:p.Ile265Met
NM_001242889.1:c.750C>G (DDC) NP_001229818.1:p.Ile250Met
XM_005271745.3:c.915C>G (DDC) XP_005271802.1:p.Ile305Met
XM_011515161.1:c.678C>G (DDC) XP_011513463.1:p.Ile226Met
XM_005271745.4:c.915C>G (DDC) XP_005271802.1:p.Ile305Met
XM_011515161.2:c.972C>G (DDC) XP_011513463.2:p.Ile324Met
NM_001082971.2:c.1029C>G (DDC) MANE Select NP_001076440.2:p.Ile343Met
NM_000790.4:c.1029C>G (DDC) NP_000781.2:p.Ile343Met
NM_001242888.2:c.795C>G (DDC) NP_001229817.2:p.Ile265Met
NM_001242886.2:c.915C>G (DDC) NP_001229815.2:p.Ile305Met
NM_001242887.2:c.885C>G (DDC) NP_001229816.2:p.Ile295Met
NM_001242889.2:c.750C>G (DDC) NP_001229818.2:p.Ile250Met