Canonical Allele Identifier: CA2639263719

Gene: ACE

Linked Data

• gnomAD v4: 17-63488883-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488883T>A , CM000679.2:g.63488883T>A	GRCh38
NC_000017.10:g.61566244T>A , CM000679.1:g.61566244T>A	GRCh37
NC_000017.9:g.58919976T>A	NCBI36
NG_011648.1:g.16811T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2450-58T>A MANE Select	ENSP00000290866.4:n.2450-58T>A
ENST00000290863.10:c.728-58T>A	ENSP00000290863.6:n.728-58T>A
ENST00000290866.9:c.2450-58T>A	ENSP00000290866.4:n.2450-58T>A
ENST00000413513.7:c.728-58T>A	ENSP00000392247.3:n.728-58T>A
ENST00000428043.5:c.2450-58T>A	ENSP00000397593.2:n.2450-58T>A
ENST00000577647.2:c.728-58T>A	ENSP00000464149.1:n.728-58T>A
ENST00000578839.5:c.*519+92T>A	ENSP00000462110.2:n.*519+92T>A
ENST00000579204.1:c.709-58T>A	ENSP00000464629.1:n.709-58T>A
ENST00000579314.5:c.*179-58T>A	ENSP00000462599.1:n.*179-58T>A
ENST00000582005.5:c.*370-58T>A	ENSP00000462002.1:n.*370-58T>A
ENST00000582761.1:c.218-58T>A	ENSP00000462909.1:n.218-58T>A
ENST00000584865.5:n.396-58T>A
NM_000789.3:c.2450-58T>A	NP_000780.1:n.2450-58T>A
NM_001178057.1:c.728-58T>A	NP_001171528.1:n.728-58T>A
NM_152830.2:c.728-58T>A	NP_690043.1:n.728-58T>A
XM_005257110.1:c.1901-58T>A	XP_005257167.1:n.1901-58T>A
XM_006721737.2:c.788-58T>A	XP_006721800.2:n.788-58T>A
XM_006721737.3:c.788-58T>A	XP_006721800.2:n.788-58T>A
NM_000789.4:c.2450-58T>A MANE Select	NP_000780.1:n.2450-58T>A
NM_001178057.2:c.728-58T>A	NP_001171528.1:n.728-58T>A
NM_152830.3:c.728-58T>A	NP_690043.1:n.728-58T>A
NM_001382700.1:c.1883-58T>A	NP_001369629.1:n.1883-58T>A
NM_001382701.1:c.1598-58T>A	NP_001369630.1:n.1598-58T>A
NM_001382702.1:c.379+92T>A	NP_001369631.1:n.379+92T>A
NR_168483.1:n.828-58T>A