Canonical Allele Identifier: CA400558303

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566365T>C (hg19) ; chr17:g.63489004T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63489004T>C , CM000679.2:g.63489004T>C	GRCh38
NC_000017.10:g.61566365T>C , CM000679.1:g.61566365T>C	GRCh37
NC_000017.9:g.58920097T>C	NCBI36
NG_011648.1:g.16932T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2513T>C MANE Select	ENSP00000290866.4:p.Leu838Pro
ENST00000290863.10:c.791T>C	ENSP00000290863.6:p.Leu264Pro
ENST00000290866.9:c.2513T>C	ENSP00000290866.4:p.Leu838Pro
ENST00000413513.7:c.791T>C	ENSP00000392247.3:p.Leu264Pro
ENST00000428043.5:c.2513T>C	ENSP00000397593.2:p.Leu838Pro
ENST00000577647.2:c.791T>C	ENSP00000464149.1:p.Leu264Pro
ENST00000578839.5:c.*519+213T>C	ENSP00000462110.2:n.*519+213T>C
ENST00000579204.1:c.772T>C	ENSP00000464629.1:n.772T>C
ENST00000579314.5:c.*242T>C	ENSP00000462599.1:n.*242T>C
ENST00000582005.5:c.*433T>C	ENSP00000462002.1:n.*433T>C
ENST00000582761.1:c.281T>C	ENSP00000462909.1:p.Leu94Pro
ENST00000584865.5:n.459T>C
NM_000789.3:c.2513T>C	NP_000780.1:p.Leu838Pro
NM_001178057.1:c.791T>C	NP_001171528.1:p.Leu264Pro
NM_152830.2:c.791T>C	NP_690043.1:p.Leu264Pro
XM_005257110.1:c.1964T>C	XP_005257167.1:p.Leu655Pro
XM_006721737.2:c.851T>C	XP_006721800.2:p.Leu284Pro
XM_006721737.3:c.851T>C	XP_006721800.2:p.Leu284Pro
NM_000789.4:c.2513T>C MANE Select	NP_000780.1:p.Leu838Pro
NM_001178057.2:c.791T>C	NP_001171528.1:p.Leu264Pro
NM_152830.3:c.791T>C	NP_690043.1:p.Leu264Pro
NM_001382700.1:c.1946T>C	NP_001369629.1:p.Leu649Pro
NM_001382701.1:c.1661T>C	NP_001369630.1:p.Leu554Pro
NM_001382702.1:c.379+213T>C	NP_001369631.1:n.379+213T>C
NR_168483.1:n.891T>C