Canonical Allele Identifier: CA400566697

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574191G>C (hg19) ; chr17:g.63496830G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496830G>C , CM000679.2:g.63496830G>C	GRCh38
NC_000017.10:g.61574191G>C , CM000679.1:g.61574191G>C	GRCh37
NC_000017.9:g.58927923G>C	NCBI36
NG_011648.1:g.24758G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3536G>C MANE Select	ENSP00000290866.4:p.Trp1179Ser
ENST00000290863.10:c.1814G>C	ENSP00000290863.6:p.Trp605Ser
ENST00000290866.9:c.3536G>C	ENSP00000290866.4:p.Trp1179Ser
ENST00000413513.7:c.1691G>C	ENSP00000392247.3:p.Trp564Ser
ENST00000428043.5:c.3536G>C	ENSP00000397593.2:p.Trp1179Ser
ENST00000577418.5:n.546G>C
ENST00000577647.2:c.1814G>C	ENSP00000464149.1:p.Trp605Ser
ENST00000578839.5:c.*1291G>C	ENSP00000462110.2:n.*1291G>C
ENST00000579314.5:c.*1265G>C	ENSP00000462599.1:n.*1265G>C
ENST00000579409.1:c.223G>C
ENST00000582244.1:n.410G>C
NM_000789.3:c.3536G>C	NP_000780.1:p.Trp1179Ser
NM_001178057.1:c.1691G>C	NP_001171528.1:p.Trp564Ser
NM_152830.2:c.1814G>C	NP_690043.1:p.Trp605Ser
XM_005257110.1:c.2987G>C	XP_005257167.1:p.Trp996Ser
XM_006721737.2:c.1874G>C	XP_006721800.2:p.Trp625Ser
XM_006721737.3:c.1874G>C	XP_006721800.2:p.Trp625Ser
NM_000789.4:c.3536G>C MANE Select	NP_000780.1:p.Trp1179Ser
NM_001178057.2:c.1691G>C	NP_001171528.1:p.Trp564Ser
NM_152830.3:c.1814G>C	NP_690043.1:p.Trp605Ser
NM_001382700.1:c.2969G>C	NP_001369629.1:p.Trp990Ser
NM_001382701.1:c.2684G>C	NP_001369630.1:p.Trp895Ser
NM_001382702.1:c.1151G>C	NP_001369631.1:p.Trp384Ser
NR_168483.1:n.1914G>C