Canonical Allele Identifier: CA400556847

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61564404C>G (hg19) ; chr17:g.63487043C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487043C>G , CM000679.2:g.63487043C>G	GRCh38
NC_000017.10:g.61564404C>G , CM000679.1:g.61564404C>G	GRCh37
NC_000017.9:g.58918136C>G	NCBI36
NG_011648.1:g.14971C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2275C>G MANE Select	ENSP00000290866.4:p.Pro759Ala
ENST00000290863.10:c.553C>G	ENSP00000290863.6:p.Pro185Ala
ENST00000290866.9:c.2275C>G	ENSP00000290866.4:p.Pro759Ala
ENST00000413513.7:c.553C>G	ENSP00000392247.3:p.Pro185Ala
ENST00000428043.5:c.2275C>G	ENSP00000397593.2:p.Pro759Ala
ENST00000577647.2:c.553C>G	ENSP00000464149.1:p.Pro185Ala
ENST00000578839.5:c.*345C>G	ENSP00000462110.2:n.*345C>G
ENST00000579204.1:c.456C>G	ENSP00000464629.1:n.456C>G
ENST00000579314.5:c.553C>G	ENSP00000462599.1:p.Pro185Ala
ENST00000579726.5:c.837C>G
ENST00000582005.5:c.*195C>G	ENSP00000462002.1:n.*195C>G
ENST00000582761.1:c.43C>G	ENSP00000462909.1:p.Pro15Ala
ENST00000584865.5:n.221C>G
NM_000789.3:c.2275C>G	NP_000780.1:p.Pro759Ala
NM_001178057.1:c.553C>G	NP_001171528.1:p.Pro185Ala
NM_152830.2:c.553C>G	NP_690043.1:p.Pro185Ala
XM_005257110.1:c.1726C>G	XP_005257167.1:p.Pro576Ala
XM_006721737.2:c.613C>G	XP_006721800.2:p.Pro205Ala
XM_006721737.3:c.613C>G	XP_006721800.2:p.Pro205Ala
NM_000789.4:c.2275C>G MANE Select	NP_000780.1:p.Pro759Ala
NM_001178057.2:c.553C>G	NP_001171528.1:p.Pro185Ala
NM_152830.3:c.553C>G	NP_690043.1:p.Pro185Ala
NM_001382700.1:c.1708C>G	NP_001369629.1:p.Pro570Ala
NM_001382701.1:c.1423C>G	NP_001369630.1:p.Pro475Ala
NM_001382702.1:c.205C>G	NP_001369631.1:p.Pro69Ala
NR_168483.1:n.575C>G