Canonical Allele Identifier: CA400568643

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574560G>A (hg19) ; chr17:g.63497199G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497199G>A , CM000679.2:g.63497199G>A	GRCh38
NC_000017.10:g.61574560G>A , CM000679.1:g.61574560G>A	GRCh37
NC_000017.9:g.58928292G>A	NCBI36
NG_011648.1:g.25127G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3754G>A MANE Select	ENSP00000290866.4:p.Ala1252Thr
ENST00000290863.10:c.2032G>A	ENSP00000290863.6:p.Ala678Thr
ENST00000290866.9:c.3754G>A	ENSP00000290866.4:p.Ala1252Thr
ENST00000413513.7:c.1909G>A	ENSP00000392247.3:p.Ala637Thr
ENST00000428043.5:c.*176G>A	ENSP00000397593.2:n.*176G>A
ENST00000577647.2:c.1969+214G>A	ENSP00000464149.1:n.1969+214G>A
ENST00000578839.5:c.*1509G>A	ENSP00000462110.2:n.*1509G>A
ENST00000579314.5:c.*1483G>A	ENSP00000462599.1:n.*1483G>A
NM_000789.3:c.3754G>A	NP_000780.1:p.Ala1252Thr
NM_001178057.1:c.1909G>A	NP_001171528.1:p.Ala637Thr
NM_152830.2:c.2032G>A	NP_690043.1:p.Ala678Thr
XM_005257110.1:c.3205G>A	XP_005257167.1:p.Ala1069Thr
XM_006721737.2:c.2092G>A	XP_006721800.2:p.Ala698Thr
XM_006721737.3:c.2092G>A	XP_006721800.2:p.Ala698Thr
NM_000789.4:c.3754G>A MANE Select	NP_000780.1:p.Ala1252Thr
NM_001178057.2:c.1909G>A	NP_001171528.1:p.Ala637Thr
NM_152830.3:c.2032G>A	NP_690043.1:p.Ala678Thr
NM_001382700.1:c.3187G>A	NP_001369629.1:p.Ala1063Thr
NM_001382701.1:c.2902G>A	NP_001369630.1:p.Ala968Thr
NM_001382702.1:c.1369G>A	NP_001369631.1:p.Ala457Thr
NR_168483.1:n.2132G>A