Canonical Allele Identifier: CA400568622

Gene: ACE

Linked Data

• gnomAD v4: 17-63497196-G-T
• MyVariant Identifiers: chr17:g.61574557G>T (hg19) ; chr17:g.63497196G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497196G>T , CM000679.2:g.63497196G>T	GRCh38
NC_000017.10:g.61574557G>T , CM000679.1:g.61574557G>T	GRCh37
NC_000017.9:g.58928289G>T	NCBI36
NG_011648.1:g.25124G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3751G>T MANE Select	ENSP00000290866.4:p.Asp1251Tyr
ENST00000290863.10:c.2029G>T	ENSP00000290863.6:p.Asp677Tyr
ENST00000290866.9:c.3751G>T	ENSP00000290866.4:p.Asp1251Tyr
ENST00000413513.7:c.1906G>T	ENSP00000392247.3:p.Asp636Tyr
ENST00000428043.5:c.*173G>T	ENSP00000397593.2:n.*173G>T
ENST00000577647.2:c.1969+211G>T	ENSP00000464149.1:n.1969+211G>T
ENST00000578839.5:c.*1506G>T	ENSP00000462110.2:n.*1506G>T
ENST00000579314.5:c.*1480G>T	ENSP00000462599.1:n.*1480G>T
NM_000789.3:c.3751G>T	NP_000780.1:p.Asp1251Tyr
NM_001178057.1:c.1906G>T	NP_001171528.1:p.Asp636Tyr
NM_152830.2:c.2029G>T	NP_690043.1:p.Asp677Tyr
XM_005257110.1:c.3202G>T	XP_005257167.1:p.Asp1068Tyr
XM_006721737.2:c.2089G>T	XP_006721800.2:p.Asp697Tyr
XM_006721737.3:c.2089G>T	XP_006721800.2:p.Asp697Tyr
NM_000789.4:c.3751G>T MANE Select	NP_000780.1:p.Asp1251Tyr
NM_001178057.2:c.1906G>T	NP_001171528.1:p.Asp636Tyr
NM_152830.3:c.2029G>T	NP_690043.1:p.Asp677Tyr
NM_001382700.1:c.3184G>T	NP_001369629.1:p.Asp1062Tyr
NM_001382701.1:c.2899G>T	NP_001369630.1:p.Asp967Tyr
NM_001382702.1:c.1366G>T	NP_001369631.1:p.Asp456Tyr
NR_168483.1:n.2129G>T