Canonical Allele Identifier: CA2838467106

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50476661A>G , CM000669.2:g.50476661A>G GRCh38
NC_000007.13:g.50544359A>G , CM000669.1:g.50544359A>G GRCh37
NC_000007.12:g.50511853A>G NCBI36
NG_008742.1:g.93796T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000444124.7:c.1022-18T>C (DDC) MANE Select ENSP00000403644.2:n.1022-18T>C
ENST00000357936.9:c.1022-18T>C (DDC) ENSP00000350616.5:n.1022-18T>C
ENST00000426377.5:c.788-18T>C (DDC) ENSP00000395069.1:n.788-18T>C
ENST00000430300.5:c.664-18T>C (DDC)
ENST00000431062.5:c.743-18T>C (DDC) ENSP00000399184.1:n.743-18T>C
ENST00000444124.6:c.1022-18T>C (DDC) ENSP00000403644.2:n.1022-18T>C
ENST00000444733.5:c.*123-18T>C (DDC) ENSP00000393724.1:n.*123-18T>C
ENST00000494914.1:n.178-18T>C (DDC)
ENST00000613602.3:c.-10-29364T>C (FIGNL1) ENSP00000481751.1:n.-10-29364T>C
ENST00000615193.4:c.743-18T>C (DDC) ENSP00000484104.1:n.743-18T>C
ENST00000617822.4:c.878-18T>C (DDC) ENSP00000478385.1:n.878-18T>C
ENST00000622873.4:c.908-18T>C (DDC) ENSP00000479110.1:n.908-18T>C
NM_000790.3:c.1022-18T>C (DDC) NP_000781.1:n.1022-18T>C
NM_001082971.1:c.1022-18T>C (DDC) NP_001076440.1:n.1022-18T>C
NM_001242886.1:c.908-18T>C (DDC) NP_001229815.1:n.908-18T>C
NM_001242887.1:c.878-18T>C (DDC) NP_001229816.1:n.878-18T>C
NM_001242888.1:c.788-18T>C (DDC) NP_001229817.1:n.788-18T>C
NM_001242889.1:c.743-18T>C (DDC) NP_001229818.1:n.743-18T>C
XM_005271745.3:c.908-18T>C (DDC) XP_005271802.1:n.908-18T>C
XM_011515161.1:c.671-18T>C (DDC) XP_011513463.1:n.671-18T>C
XM_005271745.4:c.908-18T>C (DDC) XP_005271802.1:n.908-18T>C
XM_011515161.2:c.965-18T>C (DDC) XP_011513463.2:n.965-18T>C
NM_001082971.2:c.1022-18T>C (DDC) MANE Select NP_001076440.2:n.1022-18T>C
NM_000790.4:c.1022-18T>C (DDC) NP_000781.2:n.1022-18T>C
NM_001242888.2:c.788-18T>C (DDC) NP_001229817.2:n.788-18T>C
NM_001242886.2:c.908-18T>C (DDC) NP_001229815.2:n.908-18T>C
NM_001242887.2:c.878-18T>C (DDC) NP_001229816.2:n.878-18T>C
NM_001242889.2:c.743-18T>C (DDC) NP_001229818.2:n.743-18T>C