Canonical Allele Identifier: CA400567348

Gene: ACE

Linked Data

• gnomAD v4: 17-63496901-C-T
• MyVariant Identifiers: chr17:g.61574262C>T (hg19) ; chr17:g.63496901C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496901C>T , CM000679.2:g.63496901C>T	GRCh38
NC_000017.10:g.61574262C>T , CM000679.1:g.61574262C>T	GRCh37
NC_000017.9:g.58927994C>T	NCBI36
NG_011648.1:g.24829C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3607C>T MANE Select	ENSP00000290866.4:p.Pro1203Ser
ENST00000290863.10:c.1885C>T	ENSP00000290863.6:p.Pro629Ser
ENST00000290866.9:c.3607C>T	ENSP00000290866.4:p.Pro1203Ser
ENST00000413513.7:c.1762C>T	ENSP00000392247.3:p.Pro588Ser
ENST00000428043.5:c.3607C>T	ENSP00000397593.2:p.Pro1203Ser
ENST00000577418.5:n.617C>T
ENST00000577647.2:c.1885C>T	ENSP00000464149.1:p.Pro629Ser
ENST00000578839.5:c.*1362C>T	ENSP00000462110.2:n.*1362C>T
ENST00000579314.5:c.*1336C>T	ENSP00000462599.1:n.*1336C>T
ENST00000579409.1:c.294C>T
ENST00000582244.1:n.481C>T
NM_000789.3:c.3607C>T	NP_000780.1:p.Pro1203Ser
NM_001178057.1:c.1762C>T	NP_001171528.1:p.Pro588Ser
NM_152830.2:c.1885C>T	NP_690043.1:p.Pro629Ser
XM_005257110.1:c.3058C>T	XP_005257167.1:p.Pro1020Ser
XM_006721737.2:c.1945C>T	XP_006721800.2:p.Pro649Ser
XM_006721737.3:c.1945C>T	XP_006721800.2:p.Pro649Ser
NM_000789.4:c.3607C>T MANE Select	NP_000780.1:p.Pro1203Ser
NM_001178057.2:c.1762C>T	NP_001171528.1:p.Pro588Ser
NM_152830.3:c.1885C>T	NP_690043.1:p.Pro629Ser
NM_001382700.1:c.3040C>T	NP_001369629.1:p.Pro1014Ser
NM_001382701.1:c.2755C>T	NP_001369630.1:p.Pro919Ser
NM_001382702.1:c.1222C>T	NP_001369631.1:p.Pro408Ser
NR_168483.1:n.1985C>T