Canonical Allele Identifier: CA1706649081

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50529200_50529204delinsACACT , CM000669.2:g.50529200_50529204delinsACACT GRCh38
NC_000007.13:g.50596898_50596902delinsACACT , CM000669.1:g.50596898_50596902delinsACACT GRCh37
NC_000007.12:g.50564392_50564396delinsACACT NCBI36
NG_008742.1:g.41253_41257delinsAGTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000444124.7:c.570+4_570+8delinsAGTGT (DDC) MANE Select ENSP00000403644.2:n.570+4_570+8delinsAGTG...
ENST00000357936.9:c.570+4_570+8delinsAGTGT (DDC) ENSP00000350616.5:n.570+4_570+8delinsAGTG...
ENST00000380984.4:c.570+4_570+8delinsAGTGT (DDC) ENSP00000370371.4:n.570+4_570+8delinsAGTG...
ENST00000426377.5:c.336+4_336+8delinsAGTGT (DDC) ENSP00000395069.1:n.336+4_336+8delinsAGTG...
ENST00000430300.5:c.213-924_213-920delinsAGTGT (DDC)
ENST00000431062.5:c.435+8656_435+8660delinsAGTGT (DDC) ENSP00000399184.1:n.435+8656_435+8660deli...
ENST00000444124.6:c.570+4_570+8delinsAGTGT (DDC) ENSP00000403644.2:n.570+4_570+8delinsAGTG...
ENST00000444733.5:c.456+4_456+8delinsAGTGT (DDC) ENSP00000393724.1:n.456+4_456+8delinsAGTG...
ENST00000489162.1:n.369+4_369+8delinsAGTGT (DDC)
ENST00000613602.3:c.-11+13314_-11+13318delinsAGTGT (FIGNL1) ENSP00000481751.1:n.-11+13314_-11+13318de...
ENST00000615193.4:c.435+8656_435+8660delinsAGTGT (DDC) ENSP00000484104.1:n.435+8656_435+8660deli...
ENST00000617822.4:c.570+4_570+8delinsAGTGT (DDC) ENSP00000478385.1:n.570+4_570+8delinsAGTG...
ENST00000622873.4:c.456+4_456+8delinsAGTGT (DDC) ENSP00000479110.1:n.456+4_456+8delinsAGTG...
NM_000790.3:c.570+4_570+8delinsAGTGT (DDC) NP_000781.1:n.570+4_570+8delinsAGTGT
NM_001082971.1:c.570+4_570+8delinsAGTGT (DDC) NP_001076440.1:n.570+4_570+8delinsAGTGT
NM_001242886.1:c.456+4_456+8delinsAGTGT (DDC) NP_001229815.1:n.456+4_456+8delinsAGTGT
NM_001242887.1:c.570+4_570+8delinsAGTGT (DDC) NP_001229816.1:n.570+4_570+8delinsAGTGT
NM_001242888.1:c.336+4_336+8delinsAGTGT (DDC) NP_001229817.1:n.336+4_336+8delinsAGTGT
NM_001242889.1:c.435+8656_435+8660delinsAGTGT (DDC) NP_001229818.1:n.435+8656_435+8660delinsA...
NM_001242890.1:c.570+4_570+8delinsAGTGT (DDC) NP_001229819.1:n.570+4_570+8delinsAGTGT
XM_005271745.3:c.456+4_456+8delinsAGTGT (DDC) XP_005271802.1:n.456+4_456+8delinsAGTGT
XM_011515161.1:c.219+4_219+8delinsAGTGT (DDC) XP_011513463.1:n.219+4_219+8delinsAGTGT
XM_005271745.4:c.456+4_456+8delinsAGTGT (DDC) XP_005271802.1:n.456+4_456+8delinsAGTGT
XM_011515161.2:c.513+4_513+8delinsAGTGT (DDC) XP_011513463.2:n.513+4_513+8delinsAGTGT
NM_001082971.2:c.570+4_570+8delinsAGTGT (DDC) MANE Select NP_001076440.2:n.570+4_570+8delinsAGTGT
NM_000790.4:c.570+4_570+8delinsAGTGT (DDC) NP_000781.2:n.570+4_570+8delinsAGTGT
NM_001242888.2:c.336+4_336+8delinsAGTGT (DDC) NP_001229817.2:n.336+4_336+8delinsAGTGT
NM_001242890.2:c.570+4_570+8delinsAGTGT (DDC) NP_001229819.2:n.570+4_570+8delinsAGTGT
NM_001242886.2:c.456+4_456+8delinsAGTGT (DDC) NP_001229815.2:n.456+4_456+8delinsAGTGT
NM_001242887.2:c.570+4_570+8delinsAGTGT (DDC) NP_001229816.2:n.570+4_570+8delinsAGTGT
NM_001242889.2:c.435+8656_435+8660delinsAGTGT (DDC) NP_001229818.2:n.435+8656_435+8660delinsA...