Canonical Allele Identifier: CA400558435

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566389A>C (hg19) ; chr17:g.63489028A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63489028A>C , CM000679.2:g.63489028A>C	GRCh38
NC_000017.10:g.61566389A>C , CM000679.1:g.61566389A>C	GRCh37
NC_000017.9:g.58920121A>C	NCBI36
NG_011648.1:g.16956A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2537A>C MANE Select	ENSP00000290866.4:p.Gln846Pro
ENST00000290863.10:c.815A>C	ENSP00000290863.6:p.Gln272Pro
ENST00000290866.9:c.2537A>C	ENSP00000290866.4:p.Gln846Pro
ENST00000413513.7:c.815A>C	ENSP00000392247.3:p.Gln272Pro
ENST00000428043.5:c.2537A>C	ENSP00000397593.2:p.Gln846Pro
ENST00000577647.2:c.815A>C	ENSP00000464149.1:p.Gln272Pro
ENST00000578839.5:c.*519+237A>C	ENSP00000462110.2:n.*519+237A>C
ENST00000579204.1:c.796A>C	ENSP00000464629.1:n.796A>C
ENST00000579314.5:c.*266A>C	ENSP00000462599.1:n.*266A>C
ENST00000582005.5:c.*457A>C	ENSP00000462002.1:n.*457A>C
ENST00000582761.1:c.305A>C	ENSP00000462909.1:p.Gln102Pro
ENST00000584865.5:n.483A>C
NM_000789.3:c.2537A>C	NP_000780.1:p.Gln846Pro
NM_001178057.1:c.815A>C	NP_001171528.1:p.Gln272Pro
NM_152830.2:c.815A>C	NP_690043.1:p.Gln272Pro
XM_005257110.1:c.1988A>C	XP_005257167.1:p.Gln663Pro
XM_006721737.2:c.875A>C	XP_006721800.2:p.Gln292Pro
XM_006721737.3:c.875A>C	XP_006721800.2:p.Gln292Pro
NM_000789.4:c.2537A>C MANE Select	NP_000780.1:p.Gln846Pro
NM_001178057.2:c.815A>C	NP_001171528.1:p.Gln272Pro
NM_152830.3:c.815A>C	NP_690043.1:p.Gln272Pro
NM_001382700.1:c.1970A>C	NP_001369629.1:p.Gln657Pro
NM_001382701.1:c.1685A>C	NP_001369630.1:p.Gln562Pro
NM_001382702.1:c.379+237A>C	NP_001369631.1:n.379+237A>C
NR_168483.1:n.915A>C