Canonical Allele Identifier: CA501187974

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566354G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488993G>T , CM000679.2:g.63488993G>T	GRCh38
NC_000017.10:g.61566354G>T , CM000679.1:g.61566354G>T	GRCh37
NC_000017.9:g.58920086G>T	NCBI36
NG_011648.1:g.16921G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2502G>T MANE Select	ENSP00000290866.4:p.Leu834=
ENST00000290863.10:c.780G>T	ENSP00000290863.6:p.Leu260=
ENST00000290866.9:c.2502G>T	ENSP00000290866.4:p.Leu834=
ENST00000413513.7:c.780G>T	ENSP00000392247.3:p.Leu260=
ENST00000428043.5:c.2502G>T	ENSP00000397593.2:p.Leu834=
ENST00000577647.2:c.780G>T	ENSP00000464149.1:p.Leu260=
ENST00000578839.5:c.*519+202G>T	ENSP00000462110.2:n.*519+202G>T
ENST00000579204.1:c.761G>T	ENSP00000464629.1:n.761G>T
ENST00000579314.5:c.*231G>T	ENSP00000462599.1:n.*231G>T
ENST00000582005.5:c.*422G>T	ENSP00000462002.1:n.*422G>T
ENST00000582761.1:c.270G>T	ENSP00000462909.1:p.Leu90=
ENST00000584865.5:n.448G>T
NM_000789.3:c.2502G>T	NP_000780.1:p.Leu834=
NM_001178057.1:c.780G>T	NP_001171528.1:p.Leu260=
NM_152830.2:c.780G>T	NP_690043.1:p.Leu260=
XM_005257110.1:c.1953G>T	XP_005257167.1:p.Leu651=
XM_006721737.2:c.840G>T	XP_006721800.2:p.Leu280=
XM_006721737.3:c.840G>T	XP_006721800.2:p.Leu280=
NM_000789.4:c.2502G>T MANE Select	NP_000780.1:p.Leu834=
NM_001178057.2:c.780G>T	NP_001171528.1:p.Leu260=
NM_152830.3:c.780G>T	NP_690043.1:p.Leu260=
NM_001382700.1:c.1935G>T	NP_001369629.1:p.Leu645=
NM_001382701.1:c.1650G>T	NP_001369630.1:p.Leu550=
NM_001382702.1:c.379+202G>T	NP_001369631.1:n.379+202G>T
NR_168483.1:n.880G>T