Canonical Allele Identifier: CA15227643
Gene: ZBTB38 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.141386728A>G , CM000665.2:g.141386728A>G GRCh38
NC_000003.11:g.141105570A>G , CM000665.1:g.141105570A>G GRCh37
NC_000003.10:g.142588260A>G NCBI36
NG_021426.1:g.67516A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000321464.7:c.-171-144A>G MANE Select ENSP00000372635.5:n.-171-144A>G
ENST00000636289.1:c.-482-144A>G ENSP00000490370.1:n.-482-144A>G
ENST00000637706.1:n.550-144A>G
ENST00000503809.5:c.-199A>G ENSP00000422051.1:n.-199A>G
ENST00000507657.1:n.454-144A>G
ENST00000507722.5:c.-171-144A>G ENSP00000421037.1:n.-171-144A>G
ENST00000509842.5:c.-416-144A>G ENSP00000426931.1:n.-416-144A>G
ENST00000512276.5:n.620-144A>G
ENST00000512327.1:n.287A>G
ENST00000513249.1:n.283A>G
ENST00000513619.5:n.640-144A>G
NM_001080412.2:c.-416-144A>G NP_001073881.2:n.-416-144A>G
NM_001350099.1:c.-389A>G NP_001337028.1:n.-389A>G
XM_005247257.2:c.-171-144A>G XP_005247314.1:n.-171-144A>G
XM_017006050.2:c.-489-144A>G XP_016861539.1:n.-489-144A>G
XM_024453431.1:c.-171-144A>G XP_024309199.1:n.-171-144A>G
XM_024453432.1:c.-416-144A>G XP_024309200.1:n.-416-144A>G
XM_024453433.1:c.-416-144A>G XP_024309201.1:n.-416-144A>G
XM_024453434.1:c.-199A>G XP_024309202.1:n.-199A>G
NM_001080412.3:c.-416-144A>G NP_001073881.2:n.-416-144A>G
NM_001350099.2:c.-389A>G NP_001337028.1:n.-389A>G
NM_001376112.1:c.-171-144A>G NP_001363041.1:n.-171-144A>G
NM_001376113.1:c.-171-144A>G MANE Select NP_001363042.1:n.-171-144A>G
NM_001376114.1:c.-416-144A>G NP_001363043.1:n.-416-144A>G
NM_001376115.1:c.-171-144A>G NP_001363044.1:n.-171-144A>G
NM_001376116.1:c.-204+5241A>G NP_001363045.1:n.-204+5241A>G
NM_001376117.1:c.-269-144A>G NP_001363046.1:n.-269-144A>G
NM_001376118.1:c.-294-144A>G NP_001363047.1:n.-294-144A>G
NM_001376119.1:c.-106+16782A>G NP_001363048.1:n.-106+16782A>G
NM_001376120.1:c.-66-144A>G NP_001363049.1:n.-66-144A>G
NM_001376121.1:c.-572-144A>G NP_001363050.1:n.-572-144A>G
NM_001376122.1:c.-372-144A>G NP_001363051.1:n.-372-144A>G
NM_001376123.1:c.-539-144A>G NP_001363052.1:n.-539-144A>G
NM_001376124.1:c.-514-144A>G NP_001363053.1:n.-514-144A>G
NM_001376125.1:c.-567-144A>G NP_001363054.1:n.-567-144A>G
NM_001376126.1:c.-416-144A>G NP_001363055.1:n.-416-144A>G
NM_001376127.1:c.-171-144A>G NP_001363056.1:n.-171-144A>G
NM_001376128.1:c.-294-144A>G NP_001363057.1:n.-294-144A>G
NM_001376142.1:c.-269-144A>G NP_001363071.1:n.-269-144A>G
NM_001376143.1:c.-539-144A>G NP_001363072.1:n.-539-144A>G
NM_001376150.1:c.-482-144A>G NP_001363079.1:n.-482-144A>G
NM_001376152.1:c.-171-144A>G NP_001363081.1:n.-171-144A>G
NM_001376157.1:c.-199A>G NP_001363086.1:n.-199A>G
NM_001376158.1:c.-297A>G NP_001363087.1:n.-297A>G
NM_001376159.1:c.-322A>G NP_001363088.1:n.-322A>G
NM_001376160.1:c.-567A>G NP_001363089.1:n.-567A>G
NM_001376161.1:c.-542A>G NP_001363090.1:n.-542A>G
NM_001387941.1:c.-269-144A>G NP_001374870.1:n.-269-144A>G
NM_001387945.1:c.-445-144A>G NP_001374874.1:n.-445-144A>G
NM_001387947.1:c.-986-144A>G NP_001374876.1:n.-986-144A>G
NM_001387948.1:c.-442-144A>G NP_001374877.1:n.-442-144A>G
NM_001387950.1:c.-359-144A>G NP_001374879.1:n.-359-144A>G
NM_001387952.1:c.-164-144A>G NP_001374881.1:n.-164-144A>G
NM_001387953.1:c.-171-144A>G NP_001374882.1:n.-171-144A>G
NM_001387957.1:c.-106+1853A>G NP_001374886.1:n.-106+1853A>G
NM_001387959.1:c.-164-144A>G NP_001374888.1:n.-164-144A>G
NM_001387960.1:c.-633-144A>G NP_001374889.1:n.-633-144A>G
NM_001387962.1:c.-445-144A>G NP_001374891.1:n.-445-144A>G
NM_001387966.1:c.-514-144A>G NP_001374895.1:n.-514-144A>G
NM_001387967.1:c.-397-144A>G NP_001374896.1:n.-397-144A>G
NM_001387968.1:c.-322-144A>G NP_001374897.1:n.-322-144A>G
NM_001387969.1:c.-359-144A>G NP_001374898.1:n.-359-144A>G
NM_001387970.1:c.-665-144A>G NP_001374899.1:n.-665-144A>G
NM_001387971.1:c.-274-144A>G NP_001374900.1:n.-274-144A>G
NM_001387972.1:c.-618-144A>G NP_001374901.1:n.-618-144A>G
NM_001387973.1:c.-66-144A>G NP_001374902.1:n.-66-144A>G
NM_001387974.1:c.-269-144A>G NP_001374903.1:n.-269-144A>G
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