Canonical Allele Identifier: CA15462357
Gene: ZSCAN31 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.28331910C>T , CM000668.2:g.28331910C>T GRCh38
NC_000006.11:g.28299687C>T , CM000668.1:g.28299687C>T GRCh37
NC_000006.10:g.28407666C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344279.11:c.-95-2132G>A MANE Select ENSP00000345339.6:n.-95-2132G>A
ENST00000344279.10:c.-95-2132G>A ENSP00000345339.6:n.-95-2132G>A
ENST00000396838.6:c.-31-2196G>A ENSP00000380050.2:n.-31-2196G>A
ENST00000414429.5:c.-31-2196G>A ENSP00000390076.1:n.-31-2196G>A
ENST00000414431.1:c.-97+375G>A ENSP00000407529.1:n.-97+375G>A
ENST00000426434.1:c.34-4377G>A ENSP00000398680.1:n.34-4377G>A
ENST00000426756.5:c.-95-2132G>A ENSP00000406376.1:n.-95-2132G>A
ENST00000434036.5:c.-31-2196G>A ENSP00000416225.1:n.-31-2196G>A
ENST00000435857.5:c.-97+4172G>A ENSP00000391235.1:n.-97+4172G>A
ENST00000439158.5:c.-95-2132G>A ENSP00000413705.1:n.-95-2132G>A
ENST00000439628.5:c.-31-2196G>A ENSP00000392552.1:n.-31-2196G>A
ENST00000439636.5:c.-31-2196G>A ENSP00000412519.1:n.-31-2196G>A
ENST00000444081.5:c.-31-2196G>A ENSP00000415040.1:n.-31-2196G>A
ENST00000446222.5:c.-95-2132G>A ENSP00000411033.1:n.-95-2132G>A
ENST00000446474.5:c.-97+3920G>A ENSP00000402937.1:n.-97+3920G>A
ENST00000447021.1:c.-31-2196G>A ENSP00000416108.1:n.-31-2196G>A
ENST00000453745.5:c.-31-2196G>A ENSP00000389479.1:n.-31-2196G>A
ENST00000611469.4:c.-97+375G>A ENSP00000480254.1:n.-97+375G>A
NM_001135216.1:c.-95-2132G>A NP_001128688.1:n.-95-2132G>A
NM_001243241.1:c.-31-2196G>A NP_001230170.1:n.-31-2196G>A
NM_001243242.1:c.-97+375G>A NP_001230171.1:n.-97+375G>A
NM_001243243.1:c.-97+3920G>A NP_001230172.1:n.-97+3920G>A
NM_001243244.1:c.-97+4172G>A NP_001230173.1:n.-97+4172G>A
NM_030899.4:c.-95-2132G>A NP_112161.3:n.-95-2132G>A
XM_005249295.1:c.-95-2132G>A XP_005249352.1:n.-95-2132G>A
XM_005249296.3:c.-31-2196G>A XP_005249353.1:n.-31-2196G>A
XM_011514807.1:c.-31-2196G>A XP_011513109.1:n.-31-2196G>A
XM_011514808.1:c.-31-2196G>A XP_011513110.1:n.-31-2196G>A
XM_011514809.1:c.-95-2132G>A XP_011513111.1:n.-95-2132G>A
XM_011514810.1:c.-31-2196G>A XP_011513112.1:n.-31-2196G>A
XM_011514811.1:c.-31-2196G>A XP_011513113.1:n.-31-2196G>A
XM_011514812.1:c.-31-2196G>A XP_011513114.1:n.-31-2196G>A
XM_011514813.1:c.-31-2196G>A XP_011513115.1:n.-31-2196G>A
NM_001135215.1:c.-31-2196G>A NP_001128687.1:n.-31-2196G>A
NM_145909.2:c.-31-2196G>A NP_665916.1:n.-31-2196G>A
XM_005249296.5:c.-31-2196G>A XP_005249353.1:n.-31-2196G>A
XM_011514807.3:c.-31-2196G>A XP_011513109.1:n.-31-2196G>A
XM_011514808.3:c.-31-2196G>A XP_011513110.1:n.-31-2196G>A
XM_011514811.2:c.-31-2196G>A XP_011513113.1:n.-31-2196G>A
XM_011514812.2:c.-31-2196G>A XP_011513114.1:n.-31-2196G>A
XM_011514813.2:c.-31-2196G>A XP_011513115.1:n.-31-2196G>A
XM_017011196.2:c.-31-2196G>A XP_016866685.1:n.-31-2196G>A
XM_024446521.1:c.34-4377G>A XP_024302289.1:n.34-4377G>A
XM_024446522.1:c.-96-4377G>A XP_024302290.1:n.-96-4377G>A
XM_024446523.1:c.-96-4377G>A XP_024302291.1:n.-96-4377G>A
XR_002956295.1:n.72-2132G>A
XR_002956296.1:n.721-2196G>A
NM_145909.3:c.-31-2196G>A NP_665916.1:n.-31-2196G>A
NM_030899.5:c.-95-2132G>A MANE Select NP_112161.3:n.-95-2132G>A
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