Canonical Allele Identifier: CA13819834
Gene: DCT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94456247C>T , CM000675.2:g.94456247C>T GRCh38
NC_000013.10:g.95108501C>T , CM000675.1:g.95108501C>T GRCh37
NC_000013.9:g.93906502C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377028.10:c.1179+3844G>A MANE Select ENSP00000366227.4:n.1179+3844G>A
ENST00000377028.9:c.1179+3844G>A ENSP00000366227.4:n.1179+3844G>A
ENST00000446125.1:c.1180-3585G>A ENSP00000392762.1:n.1180-3585G>A
ENST00000483392.6:c.609+3844G>A ENSP00000431275.2:n.609+3844G>A
NM_001129889.1:c.1180-3585G>A NP_001123361.1:n.1180-3585G>A
NM_001922.3:c.1179+3844G>A NP_001913.2:n.1179+3844G>A
XM_011521049.1:c.990+3844G>A XP_011519351.1:n.990+3844G>A
XM_011521050.1:c.990+3844G>A XP_011519352.1:n.990+3844G>A
XR_931610.1:n.1611+3844G>A
NM_001129889.2:c.1180-3585G>A NP_001123361.1:n.1180-3585G>A
NM_001322182.1:c.246+3844G>A NP_001309111.1:n.246+3844G>A
NM_001322183.1:c.246+3844G>A NP_001309112.1:n.246+3844G>A
NM_001322184.1:c.246+3844G>A NP_001309113.1:n.246+3844G>A
NM_001322185.1:c.246+3844G>A NP_001309114.1:n.246+3844G>A
NM_001322186.1:c.990+3844G>A NP_001309115.1:n.990+3844G>A
NM_001922.4:c.1179+3844G>A NP_001913.2:n.1179+3844G>A
XM_011521049.2:c.990+3844G>A XP_011519351.1:n.990+3844G>A
XM_017020401.2:c.1180-3585G>A XP_016875890.1:n.1180-3585G>A
XM_024449328.1:c.246+3844G>A XP_024305096.1:n.246+3844G>A
XR_002957452.1:n.1416+3844G>A
NM_001922.5:c.1179+3844G>A MANE Select NP_001913.2:n.1179+3844G>A
NM_001322182.2:c.246+3844G>A NP_001309111.1:n.246+3844G>A
NM_001322183.2:c.246+3844G>A NP_001309112.1:n.246+3844G>A
NM_001322184.2:c.246+3844G>A NP_001309113.1:n.246+3844G>A
NM_001322185.2:c.246+3844G>A NP_001309114.1:n.246+3844G>A
NM_001322186.2:c.990+3844G>A NP_001309115.1:n.990+3844G>A
NM_001129889.3:c.1180-3585G>A NP_001123361.1:n.1180-3585G>A
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