Canonical Allele Identifier: CA400568710

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574569G>A (hg19) ; chr17:g.63497208G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497208G>A , CM000679.2:g.63497208G>A	GRCh38
NC_000017.10:g.61574569G>A , CM000679.1:g.61574569G>A	GRCh37
NC_000017.9:g.58928301G>A	NCBI36
NG_011648.1:g.25136G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3763G>A MANE Select	ENSP00000290866.4:p.Ala1255Thr
ENST00000290863.10:c.2041G>A	ENSP00000290863.6:p.Ala681Thr
ENST00000290866.9:c.3763G>A	ENSP00000290866.4:p.Ala1255Thr
ENST00000413513.7:c.1918G>A	ENSP00000392247.3:p.Ala640Thr
ENST00000428043.5:c.*185G>A	ENSP00000397593.2:n.*185G>A
ENST00000577647.2:c.1969+223G>A	ENSP00000464149.1:n.1969+223G>A
ENST00000578839.5:c.*1518G>A	ENSP00000462110.2:n.*1518G>A
ENST00000579314.5:c.*1492G>A	ENSP00000462599.1:n.*1492G>A
NM_000789.3:c.3763G>A	NP_000780.1:p.Ala1255Thr
NM_001178057.1:c.1918G>A	NP_001171528.1:p.Ala640Thr
NM_152830.2:c.2041G>A	NP_690043.1:p.Ala681Thr
XM_005257110.1:c.3214G>A	XP_005257167.1:p.Ala1072Thr
XM_006721737.2:c.2101G>A	XP_006721800.2:p.Ala701Thr
XM_006721737.3:c.2101G>A	XP_006721800.2:p.Ala701Thr
NM_000789.4:c.3763G>A MANE Select	NP_000780.1:p.Ala1255Thr
NM_001178057.2:c.1918G>A	NP_001171528.1:p.Ala640Thr
NM_152830.3:c.2041G>A	NP_690043.1:p.Ala681Thr
NM_001382700.1:c.3196G>A	NP_001369629.1:p.Ala1066Thr
NM_001382701.1:c.2911G>A	NP_001369630.1:p.Ala971Thr
NM_001382702.1:c.1378G>A	NP_001369631.1:p.Ala460Thr
NR_168483.1:n.2141G>A