Canonical Allele Identifier: CA16586639
Gene: ZNF831 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.59183665A>G , CM000682.2:g.59183665A>G GRCh38
NC_000020.10:g.57758720A>G , CM000682.1:g.57758720A>G GRCh37
NC_000020.9:g.57192115A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371030.4:c.-36-7319A>G MANE Select ENSP00000360069.2:n.-36-7319A>G
ENST00000637017.1:c.-36-7319A>G ENSP00000490240.1:n.-36-7319A>G
XM_005260272.2:c.-36-7319A>G XP_005260329.1:n.-36-7319A>G
XM_005260273.2:c.-36-7319A>G XP_005260330.1:n.-36-7319A>G
XM_006723698.2:c.-36-7319A>G XP_006723761.1:n.-36-7319A>G
XM_011528533.1:c.-36-7319A>G XP_011526835.1:n.-36-7319A>G
XM_011528534.1:c.-36-7319A>G XP_011526836.1:n.-36-7319A>G
XM_011528535.1:c.-36-7319A>G XP_011526837.1:n.-36-7319A>G
XM_011528536.1:c.-36-7319A>G XP_011526838.1:n.-36-7319A>G
XM_011528537.1:c.-36-7319A>G XP_011526839.1:n.-36-7319A>G
XM_011528538.1:c.-37+685A>G XP_011526840.1:n.-37+685A>G
XM_011528539.1:c.-36-7319A>G XP_011526841.1:n.-36-7319A>G
XM_011528540.1:c.-36-7319A>G XP_011526842.1:n.-36-7319A>G
XM_005260272.3:c.-36-7319A>G XP_005260329.1:n.-36-7319A>G
XM_005260273.3:c.-36-7319A>G XP_005260330.1:n.-36-7319A>G
XM_006723698.3:c.-36-7319A>G XP_006723761.1:n.-36-7319A>G
XM_011528534.2:c.-36-7319A>G XP_011526836.1:n.-36-7319A>G
XM_011528536.2:c.-36-7319A>G XP_011526838.1:n.-36-7319A>G
XM_011528537.2:c.-36-7319A>G XP_011526839.1:n.-36-7319A>G
XM_011528538.2:c.-37+685A>G XP_011526840.1:n.-37+685A>G
XM_011528540.2:c.-36-7319A>G XP_011526842.1:n.-36-7319A>G
XM_017027642.1:c.-36-7319A>G XP_016883131.1:n.-36-7319A>G
XM_017027643.1:c.-36-7319A>G XP_016883132.1:n.-36-7319A>G
XM_017027644.1:c.-36-7319A>G XP_016883133.1:n.-36-7319A>G
NM_001384354.1:c.-36-7319A>G NP_001371283.1:n.-36-7319A>G
NM_178457.3:c.-36-7319A>G MANE Select NP_848552.1:n.-36-7319A>G
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