Canonical Allele Identifier: CA400568342

Gene: ACE

Linked Data

• gnomAD v4: 17-63497151-C-A
• MyVariant Identifiers: chr17:g.61574512C>A (hg19) ; chr17:g.63497151C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497151C>A , CM000679.2:g.63497151C>A	GRCh38
NC_000017.10:g.61574512C>A , CM000679.1:g.61574512C>A	GRCh37
NC_000017.9:g.58928244C>A	NCBI36
NG_011648.1:g.25079C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3706C>A MANE Select	ENSP00000290866.4:p.Pro1236Thr
ENST00000290863.10:c.1984C>A	ENSP00000290863.6:p.Pro662Thr
ENST00000290866.9:c.3706C>A	ENSP00000290866.4:p.Pro1236Thr
ENST00000413513.7:c.1861C>A	ENSP00000392247.3:p.Pro621Thr
ENST00000428043.5:c.*128C>A	ENSP00000397593.2:n.*128C>A
ENST00000577418.5:n.716C>A
ENST00000577647.2:c.1969+166C>A	ENSP00000464149.1:n.1969+166C>A
ENST00000578839.5:c.*1461C>A	ENSP00000462110.2:n.*1461C>A
ENST00000579314.5:c.*1435C>A	ENSP00000462599.1:n.*1435C>A
ENST00000579409.1:c.544C>A
NM_000789.3:c.3706C>A	NP_000780.1:p.Pro1236Thr
NM_001178057.1:c.1861C>A	NP_001171528.1:p.Pro621Thr
NM_152830.2:c.1984C>A	NP_690043.1:p.Pro662Thr
XM_005257110.1:c.3157C>A	XP_005257167.1:p.Pro1053Thr
XM_006721737.2:c.2044C>A	XP_006721800.2:p.Pro682Thr
XM_006721737.3:c.2044C>A	XP_006721800.2:p.Pro682Thr
NM_000789.4:c.3706C>A MANE Select	NP_000780.1:p.Pro1236Thr
NM_001178057.2:c.1861C>A	NP_001171528.1:p.Pro621Thr
NM_152830.3:c.1984C>A	NP_690043.1:p.Pro662Thr
NM_001382700.1:c.3139C>A	NP_001369629.1:p.Pro1047Thr
NM_001382701.1:c.2854C>A	NP_001369630.1:p.Pro952Thr
NM_001382702.1:c.1321C>A	NP_001369631.1:p.Pro441Thr
NR_168483.1:n.2084C>A