Canonical Allele Identifier: CA2221534677
Gene: HEATR3 HGNC NCBI

Linked Data

dbSNP Id: rs2036573153

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50069864G>A , CM000678.2:g.50069864G>A GRCh38
NC_000016.9:g.50103775G>A , CM000678.1:g.50103775G>A GRCh37
NC_000016.8:g.48661276G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000685571.1:n.639-314G>A
ENST00000689598.1:c.231-314G>A
ENST00000690683.1:n.476+3325G>A
ENST00000691270.1:n.252-314G>A
ENST00000691604.1:n.383-314G>A
ENST00000692328.1:c.400-314G>A ENSP00000510114.1:n.400-314G>A
ENST00000693352.1:c.237-314G>A
ENST00000693599.1:n.117+3325G>A
ENST00000299192.8:c.400-314G>A MANE Select ENSP00000299192.7:n.400-314G>A
ENST00000299192.7:c.400-314G>A ENSP00000299192.7:n.400-314G>A
ENST00000561819.1:n.408-314G>A
NM_182922.2:c.400-314G>A NP_891552.1:n.400-314G>A
XM_005256013.1:c.142-314G>A XP_005256070.1:n.142-314G>A
XM_011523188.1:c.49-314G>A XP_011521490.1:n.49-314G>A
XM_011523189.1:c.-61-280G>A XP_011521491.1:n.-61-280G>A
NM_001329729.1:c.49-314G>A NP_001316658.1:n.49-314G>A
NM_001329730.1:c.49-314G>A NP_001316659.1:n.49-314G>A
NM_001329731.1:c.-184-314G>A NP_001316660.1:n.-184-314G>A
NM_182922.3:c.400-314G>A NP_891552.1:n.400-314G>A
NR_138092.1:n.591-314G>A
NR_138093.1:n.591-314G>A
XM_005256013.2:c.142-314G>A XP_005256070.1:n.142-314G>A
XM_017023386.1:c.-184-314G>A XP_016878875.1:n.-184-314G>A
XR_002957828.1:n.591-314G>A
NM_182922.4:c.400-314G>A MANE Select NP_891552.1:n.400-314G>A
NM_001329729.2:c.49-314G>A NP_001316658.1:n.49-314G>A
NM_001329730.2:c.49-314G>A NP_001316659.1:n.49-314G>A
NM_001329731.2:c.-184-314G>A NP_001316660.1:n.-184-314G>A
NR_138092.2:n.562-314G>A
NR_138093.2:n.562-314G>A