Canonical Allele Identifier: CA400566458

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574157A>C (hg19) ; chr17:g.63496796A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496796A>C , CM000679.2:g.63496796A>C	GRCh38
NC_000017.10:g.61574157A>C , CM000679.1:g.61574157A>C	GRCh37
NC_000017.9:g.58927889A>C	NCBI36
NG_011648.1:g.24724A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3504-2A>C MANE Select	ENSP00000290866.4:n.3504-2A>C
ENST00000290863.10:c.1782-2A>C	ENSP00000290863.6:n.1782-2A>C
ENST00000290866.9:c.3504-2A>C	ENSP00000290866.4:n.3504-2A>C
ENST00000413513.7:c.1659-2A>C	ENSP00000392247.3:n.1659-2A>C
ENST00000428043.5:c.3504-2A>C	ENSP00000397593.2:n.3504-2A>C
ENST00000577418.5:n.514-2A>C
ENST00000577647.2:c.1782-2A>C	ENSP00000464149.1:n.1782-2A>C
ENST00000578839.5:c.*1259-2A>C	ENSP00000462110.2:n.*1259-2A>C
ENST00000579314.5:c.*1233-2A>C	ENSP00000462599.1:n.*1233-2A>C
ENST00000579409.1:c.191-2A>C
ENST00000582244.1:n.378-2A>C
NM_000789.3:c.3504-2A>C	NP_000780.1:n.3504-2A>C
NM_001178057.1:c.1659-2A>C	NP_001171528.1:n.1659-2A>C
NM_152830.2:c.1782-2A>C	NP_690043.1:n.1782-2A>C
XM_005257110.1:c.2955-2A>C	XP_005257167.1:n.2955-2A>C
XM_006721737.2:c.1842-2A>C	XP_006721800.2:n.1842-2A>C
XM_006721737.3:c.1842-2A>C	XP_006721800.2:n.1842-2A>C
NM_000789.4:c.3504-2A>C MANE Select	NP_000780.1:n.3504-2A>C
NM_001178057.2:c.1659-2A>C	NP_001171528.1:n.1659-2A>C
NM_152830.3:c.1782-2A>C	NP_690043.1:n.1782-2A>C
NM_001382700.1:c.2937-2A>C	NP_001369629.1:n.2937-2A>C
NM_001382701.1:c.2652-2A>C	NP_001369630.1:n.2652-2A>C
NM_001382702.1:c.1119-2A>C	NP_001369631.1:n.1119-2A>C
NR_168483.1:n.1882-2A>C