Canonical Allele Identifier: CA2639263377

Gene: ACE

Linked Data

• gnomAD v4: 17-63487127-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487130del , CM000679.2:g.63487130del	GRCh38
NC_000017.10:g.61564491del , CM000679.1:g.61564491del	GRCh37
NC_000017.9:g.58918223del	NCBI36
NG_011648.1:g.15058del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2305+57del MANE Select	ENSP00000290866.4:n.2305+57del
ENST00000290863.10:c.583+57del	ENSP00000290863.6:n.583+57del
ENST00000290866.9:c.2305+57del	ENSP00000290866.4:n.2305+57del
ENST00000413513.7:c.583+57del	ENSP00000392247.3:n.583+57del
ENST00000428043.5:c.2305+57del	ENSP00000397593.2:n.2305+57del
ENST00000577647.2:c.583+57del	ENSP00000464149.1:n.583+57del
ENST00000578839.5:c.*375+57del	ENSP00000462110.2:n.*375+57del
ENST00000579204.1:c.486+57del	ENSP00000464629.1:n.486+57del
ENST00000579314.5:c.583+57del	ENSP00000462599.1:n.583+57del
ENST00000582005.5:c.*225+57del	ENSP00000462002.1:n.*225+57del
ENST00000582761.1:c.73+57del	ENSP00000462909.1:n.73+57del
ENST00000584865.5:n.251+57del
NM_000789.3:c.2305+57del	NP_000780.1:n.2305+57del
NM_001178057.1:c.583+57del	NP_001171528.1:n.583+57del
NM_152830.2:c.583+57del	NP_690043.1:n.583+57del
XM_005257110.1:c.1756+57del	XP_005257167.1:n.1756+57del
XM_006721737.2:c.643+57del	XP_006721800.2:n.643+57del
XM_006721737.3:c.643+57del	XP_006721800.2:n.643+57del
NM_000789.4:c.2305+57del MANE Select	NP_000780.1:n.2305+57del
NM_001178057.2:c.583+57del	NP_001171528.1:n.583+57del
NM_152830.3:c.583+57del	NP_690043.1:n.583+57del
NM_001382700.1:c.1738+57del	NP_001369629.1:n.1738+57del
NM_001382701.1:c.1453+57del	NP_001369630.1:n.1453+57del
NM_001382702.1:c.235+57del	NP_001369631.1:n.235+57del
NR_168483.1:n.605+57del