Canonical Allele Identifier: CA400557969

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566096T>C (hg19) ; chr17:g.63488735T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488735T>C , CM000679.2:g.63488735T>C	GRCh38
NC_000017.10:g.61566096T>C , CM000679.1:g.61566096T>C	GRCh37
NC_000017.9:g.58919828T>C	NCBI36
NG_011648.1:g.16663T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2393T>C MANE Select	ENSP00000290866.4:p.Ile798Thr
ENST00000290863.10:c.671T>C	ENSP00000290863.6:p.Ile224Thr
ENST00000290866.9:c.2393T>C	ENSP00000290866.4:p.Ile798Thr
ENST00000413513.7:c.671T>C	ENSP00000392247.3:p.Ile224Thr
ENST00000428043.5:c.2393T>C	ENSP00000397593.2:p.Ile798Thr
ENST00000577647.2:c.671T>C	ENSP00000464149.1:p.Ile224Thr
ENST00000578839.5:c.*463T>C	ENSP00000462110.2:n.*463T>C
ENST00000579204.1:c.652T>C	ENSP00000464629.1:n.652T>C
ENST00000579314.5:c.*122T>C	ENSP00000462599.1:n.*122T>C
ENST00000582005.5:c.*313T>C	ENSP00000462002.1:n.*313T>C
ENST00000582761.1:c.161T>C	ENSP00000462909.1:p.Ile54Thr
ENST00000584865.5:n.339T>C
NM_000789.3:c.2393T>C	NP_000780.1:p.Ile798Thr
NM_001178057.1:c.671T>C	NP_001171528.1:p.Ile224Thr
NM_152830.2:c.671T>C	NP_690043.1:p.Ile224Thr
XM_005257110.1:c.1844T>C	XP_005257167.1:p.Ile615Thr
XM_006721737.2:c.731T>C	XP_006721800.2:p.Ile244Thr
XM_006721737.3:c.731T>C	XP_006721800.2:p.Ile244Thr
NM_000789.4:c.2393T>C MANE Select	NP_000780.1:p.Ile798Thr
NM_001178057.2:c.671T>C	NP_001171528.1:p.Ile224Thr
NM_152830.3:c.671T>C	NP_690043.1:p.Ile224Thr
NM_001382700.1:c.1826T>C	NP_001369629.1:p.Ile609Thr
NM_001382701.1:c.1541T>C	NP_001369630.1:p.Ile514Thr
NM_001382702.1:c.323T>C	NP_001369631.1:p.Ile108Thr
NR_168483.1:n.771T>C