Canonical Allele Identifier: CA400556838

Gene: ACE

Linked Data

• dbSNP Id: rs1599146831
• MyVariant Identifiers: chr17:g.61564402A>C (hg19) ; chr17:g.63487041A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487041A>C , CM000679.2:g.63487041A>C	GRCh38
NC_000017.10:g.61564402A>C , CM000679.1:g.61564402A>C	GRCh37
NC_000017.9:g.58918134A>C	NCBI36
NG_011648.1:g.14969A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2273A>C MANE Select	ENSP00000290866.4:p.His758Pro
ENST00000290863.10:c.551A>C	ENSP00000290863.6:p.His184Pro
ENST00000290866.9:c.2273A>C	ENSP00000290866.4:p.His758Pro
ENST00000413513.7:c.551A>C	ENSP00000392247.3:p.His184Pro
ENST00000428043.5:c.2273A>C	ENSP00000397593.2:p.His758Pro
ENST00000577647.2:c.551A>C	ENSP00000464149.1:p.His184Pro
ENST00000578839.5:c.*343A>C	ENSP00000462110.2:n.*343A>C
ENST00000579204.1:c.454A>C	ENSP00000464629.1:n.454A>C
ENST00000579314.5:c.551A>C	ENSP00000462599.1:p.His184Pro
ENST00000579726.5:c.835A>C
ENST00000582005.5:c.*193A>C	ENSP00000462002.1:n.*193A>C
ENST00000582761.1:c.41A>C	ENSP00000462909.1:p.His14Pro
ENST00000584865.5:n.219A>C
NM_000789.3:c.2273A>C	NP_000780.1:p.His758Pro
NM_001178057.1:c.551A>C	NP_001171528.1:p.His184Pro
NM_152830.2:c.551A>C	NP_690043.1:p.His184Pro
XM_005257110.1:c.1724A>C	XP_005257167.1:p.His575Pro
XM_006721737.2:c.611A>C	XP_006721800.2:p.His204Pro
XM_006721737.3:c.611A>C	XP_006721800.2:p.His204Pro
NM_000789.4:c.2273A>C MANE Select	NP_000780.1:p.His758Pro
NM_001178057.2:c.551A>C	NP_001171528.1:p.His184Pro
NM_152830.3:c.551A>C	NP_690043.1:p.His184Pro
NM_001382700.1:c.1706A>C	NP_001369629.1:p.His569Pro
NM_001382701.1:c.1421A>C	NP_001369630.1:p.His474Pro
NM_001382702.1:c.203A>C	NP_001369631.1:p.His68Pro
NR_168483.1:n.573A>C