Canonical Allele Identifier: CA400557930

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566077G>T (hg19) ; chr17:g.63488716G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488716G>T , CM000679.2:g.63488716G>T	GRCh38
NC_000017.10:g.61566077G>T , CM000679.1:g.61566077G>T	GRCh37
NC_000017.9:g.58919809G>T	NCBI36
NG_011648.1:g.16644G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2374G>T MANE Select	ENSP00000290866.4:p.Asp792Tyr
ENST00000290863.10:c.652G>T	ENSP00000290863.6:p.Asp218Tyr
ENST00000290866.9:c.2374G>T	ENSP00000290866.4:p.Asp792Tyr
ENST00000413513.7:c.652G>T	ENSP00000392247.3:p.Asp218Tyr
ENST00000428043.5:c.2374G>T	ENSP00000397593.2:p.Asp792Tyr
ENST00000577647.2:c.652G>T	ENSP00000464149.1:p.Asp218Tyr
ENST00000578839.5:c.*444G>T	ENSP00000462110.2:n.*444G>T
ENST00000579204.1:c.633G>T	ENSP00000464629.1:n.633G>T
ENST00000579314.5:c.*103G>T	ENSP00000462599.1:n.*103G>T
ENST00000582005.5:c.*294G>T	ENSP00000462002.1:n.*294G>T
ENST00000582761.1:c.142G>T	ENSP00000462909.1:p.Asp48Tyr
ENST00000584865.5:n.320G>T
NM_000789.3:c.2374G>T	NP_000780.1:p.Asp792Tyr
NM_001178057.1:c.652G>T	NP_001171528.1:p.Asp218Tyr
NM_152830.2:c.652G>T	NP_690043.1:p.Asp218Tyr
XM_005257110.1:c.1825G>T	XP_005257167.1:p.Asp609Tyr
XM_006721737.2:c.712G>T	XP_006721800.2:p.Asp238Tyr
XM_006721737.3:c.712G>T	XP_006721800.2:p.Asp238Tyr
NM_000789.4:c.2374G>T MANE Select	NP_000780.1:p.Asp792Tyr
NM_001178057.2:c.652G>T	NP_001171528.1:p.Asp218Tyr
NM_152830.3:c.652G>T	NP_690043.1:p.Asp218Tyr
NM_001382700.1:c.1807G>T	NP_001369629.1:p.Asp603Tyr
NM_001382701.1:c.1522G>T	NP_001369630.1:p.Asp508Tyr
NM_001382702.1:c.304G>T	NP_001369631.1:p.Asp102Tyr
NR_168483.1:n.752G>T