Canonical Allele Identifier: CA400558207

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566343A>C (hg19) ; chr17:g.63488982A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488982A>C , CM000679.2:g.63488982A>C	GRCh38
NC_000017.10:g.61566343A>C , CM000679.1:g.61566343A>C	GRCh37
NC_000017.9:g.58920075A>C	NCBI36
NG_011648.1:g.16910A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2491A>C MANE Select	ENSP00000290866.4:p.Thr831Pro
ENST00000290863.10:c.769A>C	ENSP00000290863.6:p.Thr257Pro
ENST00000290866.9:c.2491A>C	ENSP00000290866.4:p.Thr831Pro
ENST00000413513.7:c.769A>C	ENSP00000392247.3:p.Thr257Pro
ENST00000428043.5:c.2491A>C	ENSP00000397593.2:p.Thr831Pro
ENST00000577647.2:c.769A>C	ENSP00000464149.1:p.Thr257Pro
ENST00000578839.5:c.*519+191A>C	ENSP00000462110.2:n.*519+191A>C
ENST00000579204.1:c.750A>C	ENSP00000464629.1:n.750A>C
ENST00000579314.5:c.*220A>C	ENSP00000462599.1:n.*220A>C
ENST00000582005.5:c.*411A>C	ENSP00000462002.1:n.*411A>C
ENST00000582761.1:c.259A>C	ENSP00000462909.1:p.Thr87Pro
ENST00000584865.5:n.437A>C
NM_000789.3:c.2491A>C	NP_000780.1:p.Thr831Pro
NM_001178057.1:c.769A>C	NP_001171528.1:p.Thr257Pro
NM_152830.2:c.769A>C	NP_690043.1:p.Thr257Pro
XM_005257110.1:c.1942A>C	XP_005257167.1:p.Thr648Pro
XM_006721737.2:c.829A>C	XP_006721800.2:p.Thr277Pro
XM_006721737.3:c.829A>C	XP_006721800.2:p.Thr277Pro
NM_000789.4:c.2491A>C MANE Select	NP_000780.1:p.Thr831Pro
NM_001178057.2:c.769A>C	NP_001171528.1:p.Thr257Pro
NM_152830.3:c.769A>C	NP_690043.1:p.Thr257Pro
NM_001382700.1:c.1924A>C	NP_001369629.1:p.Thr642Pro
NM_001382701.1:c.1639A>C	NP_001369630.1:p.Thr547Pro
NM_001382702.1:c.379+191A>C	NP_001369631.1:n.379+191A>C
NR_168483.1:n.869A>C