Canonical Allele Identifier: CA400567322

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574259A>T (hg19) ; chr17:g.63496898A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496898A>T , CM000679.2:g.63496898A>T	GRCh38
NC_000017.10:g.61574259A>T , CM000679.1:g.61574259A>T	GRCh37
NC_000017.9:g.58927991A>T	NCBI36
NG_011648.1:g.24826A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3604A>T MANE Select	ENSP00000290866.4:p.Lys1202Ter
ENST00000290863.10:c.1882A>T	ENSP00000290863.6:p.Lys628Ter
ENST00000290866.9:c.3604A>T	ENSP00000290866.4:p.Lys1202Ter
ENST00000413513.7:c.1759A>T	ENSP00000392247.3:p.Lys587Ter
ENST00000428043.5:c.3604A>T	ENSP00000397593.2:p.Lys1202Ter
ENST00000577418.5:n.614A>T
ENST00000577647.2:c.1882A>T	ENSP00000464149.1:p.Lys628Ter
ENST00000578839.5:c.*1359A>T	ENSP00000462110.2:n.*1359A>T
ENST00000579314.5:c.*1333A>T	ENSP00000462599.1:n.*1333A>T
ENST00000579409.1:c.291A>T
ENST00000582244.1:n.478A>T
NM_000789.3:c.3604A>T	NP_000780.1:p.Lys1202Ter
NM_001178057.1:c.1759A>T	NP_001171528.1:p.Lys587Ter
NM_152830.2:c.1882A>T	NP_690043.1:p.Lys628Ter
XM_005257110.1:c.3055A>T	XP_005257167.1:p.Lys1019Ter
XM_006721737.2:c.1942A>T	XP_006721800.2:p.Lys648Ter
XM_006721737.3:c.1942A>T	XP_006721800.2:p.Lys648Ter
NM_000789.4:c.3604A>T MANE Select	NP_000780.1:p.Lys1202Ter
NM_001178057.2:c.1759A>T	NP_001171528.1:p.Lys587Ter
NM_152830.3:c.1882A>T	NP_690043.1:p.Lys628Ter
NM_001382700.1:c.3037A>T	NP_001369629.1:p.Lys1013Ter
NM_001382701.1:c.2752A>T	NP_001369630.1:p.Lys918Ter
NM_001382702.1:c.1219A>T	NP_001369631.1:p.Lys407Ter
NR_168483.1:n.1982A>T