Canonical Allele Identifier: CA501187966

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566348A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488987A>C , CM000679.2:g.63488987A>C	GRCh38
NC_000017.10:g.61566348A>C , CM000679.1:g.61566348A>C	GRCh37
NC_000017.9:g.58920080A>C	NCBI36
NG_011648.1:g.16915A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2496A>C MANE Select	ENSP00000290866.4:p.Pro832=
ENST00000290863.10:c.774A>C	ENSP00000290863.6:p.Pro258=
ENST00000290866.9:c.2496A>C	ENSP00000290866.4:p.Pro832=
ENST00000413513.7:c.774A>C	ENSP00000392247.3:p.Pro258=
ENST00000428043.5:c.2496A>C	ENSP00000397593.2:p.Pro832=
ENST00000577647.2:c.774A>C	ENSP00000464149.1:p.Pro258=
ENST00000578839.5:c.*519+196A>C	ENSP00000462110.2:n.*519+196A>C
ENST00000579204.1:c.755A>C	ENSP00000464629.1:n.755A>C
ENST00000579314.5:c.*225A>C	ENSP00000462599.1:n.*225A>C
ENST00000582005.5:c.*416A>C	ENSP00000462002.1:n.*416A>C
ENST00000582761.1:c.264A>C	ENSP00000462909.1:p.Pro88=
ENST00000584865.5:n.442A>C
NM_000789.3:c.2496A>C	NP_000780.1:p.Pro832=
NM_001178057.1:c.774A>C	NP_001171528.1:p.Pro258=
NM_152830.2:c.774A>C	NP_690043.1:p.Pro258=
XM_005257110.1:c.1947A>C	XP_005257167.1:p.Pro649=
XM_006721737.2:c.834A>C	XP_006721800.2:p.Pro278=
XM_006721737.3:c.834A>C	XP_006721800.2:p.Pro278=
NM_000789.4:c.2496A>C MANE Select	NP_000780.1:p.Pro832=
NM_001178057.2:c.774A>C	NP_001171528.1:p.Pro258=
NM_152830.3:c.774A>C	NP_690043.1:p.Pro258=
NM_001382700.1:c.1929A>C	NP_001369629.1:p.Pro643=
NM_001382701.1:c.1644A>C	NP_001369630.1:p.Pro548=
NM_001382702.1:c.379+196A>C	NP_001369631.1:n.379+196A>C
NR_168483.1:n.874A>C