Canonical Allele Identifier: CA501186714

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566022G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488661G>C , CM000679.2:g.63488661G>C	GRCh38
NC_000017.10:g.61566022G>C , CM000679.1:g.61566022G>C	GRCh37
NC_000017.9:g.58919754G>C	NCBI36
NG_011648.1:g.16589G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2319G>C MANE Select	ENSP00000290866.4:p.Val773=
ENST00000290863.10:c.597G>C	ENSP00000290863.6:p.Val199=
ENST00000290866.9:c.2319G>C	ENSP00000290866.4:p.Val773=
ENST00000413513.7:c.597G>C	ENSP00000392247.3:p.Val199=
ENST00000428043.5:c.2319G>C	ENSP00000397593.2:p.Val773=
ENST00000577647.2:c.597G>C	ENSP00000464149.1:p.Val199=
ENST00000578839.5:c.*389G>C	ENSP00000462110.2:n.*389G>C
ENST00000579204.1:c.578G>C	ENSP00000464629.1:n.578G>C
ENST00000579314.5:c.*48G>C	ENSP00000462599.1:n.*48G>C
ENST00000582005.5:c.*239G>C	ENSP00000462002.1:n.*239G>C
ENST00000582761.1:c.87G>C	ENSP00000462909.1:p.Val29=
ENST00000584865.5:n.265G>C
NM_000789.3:c.2319G>C	NP_000780.1:p.Val773=
NM_001178057.1:c.597G>C	NP_001171528.1:p.Val199=
NM_152830.2:c.597G>C	NP_690043.1:p.Val199=
XM_005257110.1:c.1770G>C	XP_005257167.1:p.Val590=
XM_006721737.2:c.657G>C	XP_006721800.2:p.Val219=
XM_006721737.3:c.657G>C	XP_006721800.2:p.Val219=
NM_000789.4:c.2319G>C MANE Select	NP_000780.1:p.Val773=
NM_001178057.2:c.597G>C	NP_001171528.1:p.Val199=
NM_152830.3:c.597G>C	NP_690043.1:p.Val199=
NM_001382700.1:c.1752G>C	NP_001369629.1:p.Val584=
NM_001382701.1:c.1467G>C	NP_001369630.1:p.Val489=
NM_001382702.1:c.249G>C	NP_001369631.1:p.Val83=
NR_168483.1:n.697G>C