Canonical Allele Identifier: CA400558237

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566358C>G (hg19) ; chr17:g.63488997C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488997C>G , CM000679.2:g.63488997C>G	GRCh38
NC_000017.10:g.61566358C>G , CM000679.1:g.61566358C>G	GRCh37
NC_000017.9:g.58920090C>G	NCBI36
NG_011648.1:g.16925C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2506C>G MANE Select	ENSP00000290866.4:p.Gln836Glu
ENST00000290863.10:c.784C>G	ENSP00000290863.6:p.Gln262Glu
ENST00000290866.9:c.2506C>G	ENSP00000290866.4:p.Gln836Glu
ENST00000413513.7:c.784C>G	ENSP00000392247.3:p.Gln262Glu
ENST00000428043.5:c.2506C>G	ENSP00000397593.2:p.Gln836Glu
ENST00000577647.2:c.784C>G	ENSP00000464149.1:p.Gln262Glu
ENST00000578839.5:c.*519+206C>G	ENSP00000462110.2:n.*519+206C>G
ENST00000579204.1:c.765C>G	ENSP00000464629.1:n.765C>G
ENST00000579314.5:c.*235C>G	ENSP00000462599.1:n.*235C>G
ENST00000582005.5:c.*426C>G	ENSP00000462002.1:n.*426C>G
ENST00000582761.1:c.274C>G	ENSP00000462909.1:p.Gln92Glu
ENST00000584865.5:n.452C>G
NM_000789.3:c.2506C>G	NP_000780.1:p.Gln836Glu
NM_001178057.1:c.784C>G	NP_001171528.1:p.Gln262Glu
NM_152830.2:c.784C>G	NP_690043.1:p.Gln262Glu
XM_005257110.1:c.1957C>G	XP_005257167.1:p.Gln653Glu
XM_006721737.2:c.844C>G	XP_006721800.2:p.Gln282Glu
XM_006721737.3:c.844C>G	XP_006721800.2:p.Gln282Glu
NM_000789.4:c.2506C>G MANE Select	NP_000780.1:p.Gln836Glu
NM_001178057.2:c.784C>G	NP_001171528.1:p.Gln262Glu
NM_152830.3:c.784C>G	NP_690043.1:p.Gln262Glu
NM_001382700.1:c.1939C>G	NP_001369629.1:p.Gln647Glu
NM_001382701.1:c.1654C>G	NP_001369630.1:p.Gln552Glu
NM_001382702.1:c.379+206C>G	NP_001369631.1:n.379+206C>G
NR_168483.1:n.884C>G