Canonical Allele Identifier: CA2269941658
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs1699331571
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63480781G>A , CM000679.2:g.63480781G>A GRCh38
NC_000017.10:g.61558142G>A , CM000679.1:g.61558142G>A GRCh37
NC_000017.9:g.58911874G>A NCBI36
NG_011648.1:g.8709G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.847+253G>A MANE Select ENSP00000290866.4:n.847+253G>A
ENST00000290866.9:c.847+253G>A ENSP00000290866.4:n.847+253G>A
ENST00000428043.5:c.847+253G>A ENSP00000397593.2:n.847+253G>A
ENST00000582627.1:c.847+253G>A ENSP00000462280.1:n.847+253G>A
ENST00000582678.5:c.*246+253G>A ENSP00000462995.1:n.*246+253G>A
ENST00000584529.5:n.881+253G>A
NM_000789.3:c.847+253G>A NP_000780.1:n.847+253G>A
XM_005257110.1:c.298+253G>A XP_005257167.1:n.298+253G>A
NM_000789.4:c.847+253G>A MANE Select NP_000780.1:n.847+253G>A
NM_001382700.1:c.374+253G>A NP_001369629.1:n.374+253G>A
NM_001382701.1:c.-6+253G>A NP_001369630.1:n.-6+253G>A
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