Canonical Allele Identifier: CA2221534498
Gene: HEATR3 HGNC NCBI

Linked Data

dbSNP Id: rs2036570970

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50069778A>G , CM000678.2:g.50069778A>G GRCh38
NC_000016.9:g.50103689A>G , CM000678.1:g.50103689A>G GRCh37
NC_000016.8:g.48661190A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000685571.1:n.639-400A>G
ENST00000689598.1:c.231-400A>G
ENST00000690683.1:n.476+3239A>G
ENST00000691270.1:n.252-400A>G
ENST00000691604.1:n.383-400A>G
ENST00000692328.1:c.400-400A>G ENSP00000510114.1:n.400-400A>G
ENST00000693352.1:c.237-400A>G
ENST00000693599.1:n.117+3239A>G
ENST00000299192.8:c.400-400A>G MANE Select ENSP00000299192.7:n.400-400A>G
ENST00000299192.7:c.400-400A>G ENSP00000299192.7:n.400-400A>G
ENST00000561819.1:n.408-400A>G
NM_182922.2:c.400-400A>G NP_891552.1:n.400-400A>G
XM_005256013.1:c.142-400A>G XP_005256070.1:n.142-400A>G
XM_011523188.1:c.49-400A>G XP_011521490.1:n.49-400A>G
XM_011523189.1:c.-61-366A>G XP_011521491.1:n.-61-366A>G
NM_001329729.1:c.49-400A>G NP_001316658.1:n.49-400A>G
NM_001329730.1:c.49-400A>G NP_001316659.1:n.49-400A>G
NM_001329731.1:c.-184-400A>G NP_001316660.1:n.-184-400A>G
NM_182922.3:c.400-400A>G NP_891552.1:n.400-400A>G
NR_138092.1:n.591-400A>G
NR_138093.1:n.591-400A>G
XM_005256013.2:c.142-400A>G XP_005256070.1:n.142-400A>G
XM_017023386.1:c.-184-400A>G XP_016878875.1:n.-184-400A>G
XR_002957828.1:n.591-400A>G
NM_182922.4:c.400-400A>G MANE Select NP_891552.1:n.400-400A>G
NM_001329729.2:c.49-400A>G NP_001316658.1:n.49-400A>G
NM_001329730.2:c.49-400A>G NP_001316659.1:n.49-400A>G
NM_001329731.2:c.-184-400A>G NP_001316660.1:n.-184-400A>G
NR_138092.2:n.562-400A>G
NR_138093.2:n.562-400A>G