Canonical Allele Identifier: CA326953677
Gene: ACE2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.15579386C>T , CM000685.2:g.15579386C>T GRCh38
NC_000023.10:g.15597509C>T , CM000685.1:g.15597509C>T GRCh37
NC_000023.9:g.15507430C>T NCBI36
NG_012575.1:g.27684G>A
NG_012575.2:g.27773G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252519.8:c.1071-1071G>A MANE Select ENSP00000252519.3:n.1071-1071G>A
ENST00000427411.2:c.1071-1071G>A ENSP00000389326.1:n.1071-1071G>A
ENST00000649243.1:c.*1149-1071G>A ENSP00000497489.1:n.*1149-1071G>A
ENST00000677282.1:c.32+895G>A ENSP00000504747.1:n.32+895G>A
ENST00000678046.1:c.1071-1071G>A ENSP00000502872.1:n.1071-1071G>A
ENST00000678073.1:c.1071-1071G>A ENSP00000504103.1:n.1071-1071G>A
ENST00000679162.1:c.1071-1071G>A ENSP00000503771.1:n.1071-1071G>A
ENST00000679212.1:c.1071-1071G>A ENSP00000503558.1:n.1071-1071G>A
ENST00000679278.1:c.1071-1071G>A ENSP00000504010.1:n.1071-1071G>A
ENST00000680121.1:c.1071-1071G>A ENSP00000505992.1:n.1071-1071G>A
ENST00000252519.7:c.1071-1071G>A ENSP00000252519.3:n.1071-1071G>A
ENST00000427411.1:c.1071-1071G>A ENSP00000389326.1:n.1071-1071G>A
NM_021804.2:c.1071-1071G>A NP_068576.1:n.1071-1071G>A
XM_011545549.1:c.1071-1071G>A XP_011543851.1:n.1071-1071G>A
XM_011545550.1:c.1071-1071G>A XP_011543852.1:n.1071-1071G>A
XM_011545551.1:c.1071-1071G>A XP_011543853.1:n.1071-1071G>A
XM_011545552.1:c.1071-1071G>A XP_011543854.1:n.1071-1071G>A
XM_011545549.2:c.1071-1071G>A XP_011543851.1:n.1071-1071G>A
XM_011545551.3:c.1071-1071G>A XP_011543853.1:n.1071-1071G>A
XM_011545552.2:c.1071-1071G>A XP_011543854.1:n.1071-1071G>A
NM_001371415.1:c.1071-1071G>A MANE Select NP_001358344.1:n.1071-1071G>A
NM_021804.3:c.1071-1071G>A NP_068576.1:n.1071-1071G>A
NM_001386259.1:c.1071-1071G>A NP_001373188.1:n.1071-1071G>A
NM_001386260.1:c.1071-1071G>A NP_001373189.1:n.1071-1071G>A
NM_001388452.1:c.32+895G>A NP_001375381.1:n.32+895G>A
NM_001389402.1:c.1071-1071G>A NP_001376331.1:n.1071-1071G>A
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