Canonical Allele Identifier: CA8700642

Gene: ACE

Linked Data

• dbSNP Id: rs751737727
• ExAC: 17:61574513 C / T
• gnomAD v2: 17-61574513-C-T
• gnomAD v4: 17-63497152-C-T
• MyVariant Identifiers: chr17:g.61574513C>T (hg19) ; chr17:g.63497152C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497152C>T , CM000679.2:g.63497152C>T	GRCh38
NC_000017.10:g.61574513C>T , CM000679.1:g.61574513C>T	GRCh37
NC_000017.9:g.58928245C>T	NCBI36
NG_011648.1:g.25080C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3707C>T MANE Select	ENSP00000290866.4:p.Pro1236Leu
ENST00000290863.10:c.1985C>T	ENSP00000290863.6:p.Pro662Leu
ENST00000290866.9:c.3707C>T	ENSP00000290866.4:p.Pro1236Leu
ENST00000413513.7:c.1862C>T	ENSP00000392247.3:p.Pro621Leu
ENST00000428043.5:c.*129C>T	ENSP00000397593.2:n.*129C>T
ENST00000577418.5:n.717C>T
ENST00000577647.2:c.1969+167C>T	ENSP00000464149.1:n.1969+167C>T
ENST00000578839.5:c.*1462C>T	ENSP00000462110.2:n.*1462C>T
ENST00000579314.5:c.*1436C>T	ENSP00000462599.1:n.*1436C>T
ENST00000579409.1:c.545C>T
NM_000789.3:c.3707C>T	NP_000780.1:p.Pro1236Leu
NM_001178057.1:c.1862C>T	NP_001171528.1:p.Pro621Leu
NM_152830.2:c.1985C>T	NP_690043.1:p.Pro662Leu
XM_005257110.1:c.3158C>T	XP_005257167.1:p.Pro1053Leu
XM_006721737.2:c.2045C>T	XP_006721800.2:p.Pro682Leu
XM_006721737.3:c.2045C>T	XP_006721800.2:p.Pro682Leu
NM_000789.4:c.3707C>T MANE Select	NP_000780.1:p.Pro1236Leu
NM_001178057.2:c.1862C>T	NP_001171528.1:p.Pro621Leu
NM_152830.3:c.1985C>T	NP_690043.1:p.Pro662Leu
NM_001382700.1:c.3140C>T	NP_001369629.1:p.Pro1047Leu
NM_001382701.1:c.2855C>T	NP_001369630.1:p.Pro952Leu
NM_001382702.1:c.1322C>T	NP_001369631.1:p.Pro441Leu
NR_168483.1:n.2085C>T