Canonical Allele Identifier: CA292891005

Gene: ACE

Linked Data

• dbSNP Id: rs1024461682
• gnomAD v3: 17-63498376-G-T
• gnomAD v4: 17-63498376-G-T
• MyVariant Identifiers: chr17:g.61575737G>T (hg19) ; chr17:g.63498376G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498376G>T , CM000679.2:g.63498376G>T	GRCh38
NC_000017.10:g.61575737G>T , CM000679.1:g.61575737G>T	GRCh37
NC_000017.9:g.58929469G>T	NCBI36
NG_011648.1:g.26304G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.9:c.*1010G>T	ENSP00000290866.4:n.*1010G>T
ENST00000428043.5:c.*1353G>T	ENSP00000397593.2:n.*1353G>T
ENST00000577647.2:c.1969+1391G>T	ENSP00000464149.1:n.1969+1391G>T
NM_000789.3:c.*1010G>T	NP_000780.1:n.*1010G>T
NM_001178057.1:c.*1010G>T	NP_001171528.1:n.*1010G>T
NM_152830.2:c.*1010G>T	NP_690043.1:n.*1010G>T
XM_005257110.1:c.*1010G>T	XP_005257167.1:n.*1010G>T
XM_006721737.2:c.*1010G>T	XP_006721800.2:n.*1010G>T