Canonical Allele Identifier: CA2639263626

Gene: ACE

Linked Data

• gnomAD v4: 17-63488539-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488539C>G , CM000679.2:g.63488539C>G	GRCh38
NC_000017.10:g.61565900C>G , CM000679.1:g.61565900C>G	GRCh37
NC_000017.9:g.58919632C>G	NCBI36
NG_011648.1:g.16467C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2306-109C>G MANE Select	ENSP00000290866.4:n.2306-109C>G
ENST00000290863.10:c.584-109C>G	ENSP00000290863.6:n.584-109C>G
ENST00000290866.9:c.2306-109C>G	ENSP00000290866.4:n.2306-109C>G
ENST00000413513.7:c.584-109C>G	ENSP00000392247.3:n.584-109C>G
ENST00000428043.5:c.2306-109C>G	ENSP00000397593.2:n.2306-109C>G
ENST00000577647.2:c.584-109C>G	ENSP00000464149.1:n.584-109C>G
ENST00000578839.5:c.*376-109C>G	ENSP00000462110.2:n.*376-109C>G
ENST00000579204.1:c.487-31C>G	ENSP00000464629.1:n.487-31C>G
ENST00000579314.5:c.584-31C>G	ENSP00000462599.1:n.584-31C>G
ENST00000582005.5:c.*226-109C>G	ENSP00000462002.1:n.*226-109C>G
ENST00000582761.1:c.74-109C>G	ENSP00000462909.1:n.74-109C>G
ENST00000584865.5:n.252-109C>G
NM_000789.3:c.2306-109C>G	NP_000780.1:n.2306-109C>G
NM_001178057.1:c.584-109C>G	NP_001171528.1:n.584-109C>G
NM_152830.2:c.584-109C>G	NP_690043.1:n.584-109C>G
XM_005257110.1:c.1757-109C>G	XP_005257167.1:n.1757-109C>G
XM_006721737.2:c.644-109C>G	XP_006721800.2:n.644-109C>G
XM_006721737.3:c.644-109C>G	XP_006721800.2:n.644-109C>G
NM_000789.4:c.2306-109C>G MANE Select	NP_000780.1:n.2306-109C>G
NM_001178057.2:c.584-109C>G	NP_001171528.1:n.584-109C>G
NM_152830.3:c.584-109C>G	NP_690043.1:n.584-109C>G
NM_001382700.1:c.1739-109C>G	NP_001369629.1:n.1739-109C>G
NM_001382701.1:c.1454-109C>G	NP_001369630.1:n.1454-109C>G
NM_001382702.1:c.236-109C>G	NP_001369631.1:n.236-109C>G
NR_168483.1:n.606-31C>G