Canonical Allele Identifier: CA400557798

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566015C>A (hg19) ; chr17:g.63488654C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488654C>A , CM000679.2:g.63488654C>A	GRCh38
NC_000017.10:g.61566015C>A , CM000679.1:g.61566015C>A	GRCh37
NC_000017.9:g.58919747C>A	NCBI36
NG_011648.1:g.16582C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2312C>A MANE Select	ENSP00000290866.4:p.Thr771Lys
ENST00000290863.10:c.590C>A	ENSP00000290863.6:p.Thr197Lys
ENST00000290866.9:c.2312C>A	ENSP00000290866.4:p.Thr771Lys
ENST00000413513.7:c.590C>A	ENSP00000392247.3:p.Thr197Lys
ENST00000428043.5:c.2312C>A	ENSP00000397593.2:p.Thr771Lys
ENST00000577647.2:c.590C>A	ENSP00000464149.1:p.Thr197Lys
ENST00000578839.5:c.*382C>A	ENSP00000462110.2:n.*382C>A
ENST00000579204.1:c.571C>A	ENSP00000464629.1:n.571C>A
ENST00000579314.5:c.*41C>A	ENSP00000462599.1:n.*41C>A
ENST00000582005.5:c.*232C>A	ENSP00000462002.1:n.*232C>A
ENST00000582761.1:c.80C>A	ENSP00000462909.1:p.Thr27Lys
ENST00000584865.5:n.258C>A
NM_000789.3:c.2312C>A	NP_000780.1:p.Thr771Lys
NM_001178057.1:c.590C>A	NP_001171528.1:p.Thr197Lys
NM_152830.2:c.590C>A	NP_690043.1:p.Thr197Lys
XM_005257110.1:c.1763C>A	XP_005257167.1:p.Thr588Lys
XM_006721737.2:c.650C>A	XP_006721800.2:p.Thr217Lys
XM_006721737.3:c.650C>A	XP_006721800.2:p.Thr217Lys
NM_000789.4:c.2312C>A MANE Select	NP_000780.1:p.Thr771Lys
NM_001178057.2:c.590C>A	NP_001171528.1:p.Thr197Lys
NM_152830.3:c.590C>A	NP_690043.1:p.Thr197Lys
NM_001382700.1:c.1745C>A	NP_001369629.1:p.Thr582Lys
NM_001382701.1:c.1460C>A	NP_001369630.1:p.Thr487Lys
NM_001382702.1:c.242C>A	NP_001369631.1:p.Thr81Lys
NR_168483.1:n.690C>A