Canonical Allele Identifier: CA400558180

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566331T>A (hg19) ; chr17:g.63488970T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488970T>A , CM000679.2:g.63488970T>A	GRCh38
NC_000017.10:g.61566331T>A , CM000679.1:g.61566331T>A	GRCh37
NC_000017.9:g.58920063T>A	NCBI36
NG_011648.1:g.16898T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2479T>A MANE Select	ENSP00000290866.4:p.Ser827Thr
ENST00000290863.10:c.757T>A	ENSP00000290863.6:p.Ser253Thr
ENST00000290866.9:c.2479T>A	ENSP00000290866.4:p.Ser827Thr
ENST00000413513.7:c.757T>A	ENSP00000392247.3:p.Ser253Thr
ENST00000428043.5:c.2479T>A	ENSP00000397593.2:p.Ser827Thr
ENST00000577647.2:c.757T>A	ENSP00000464149.1:p.Ser253Thr
ENST00000578839.5:c.*519+179T>A	ENSP00000462110.2:n.*519+179T>A
ENST00000579204.1:c.738T>A	ENSP00000464629.1:n.738T>A
ENST00000579314.5:c.*208T>A	ENSP00000462599.1:n.*208T>A
ENST00000582005.5:c.*399T>A	ENSP00000462002.1:n.*399T>A
ENST00000582761.1:c.247T>A	ENSP00000462909.1:p.Ser83Thr
ENST00000584865.5:n.425T>A
NM_000789.3:c.2479T>A	NP_000780.1:p.Ser827Thr
NM_001178057.1:c.757T>A	NP_001171528.1:p.Ser253Thr
NM_152830.2:c.757T>A	NP_690043.1:p.Ser253Thr
XM_005257110.1:c.1930T>A	XP_005257167.1:p.Ser644Thr
XM_006721737.2:c.817T>A	XP_006721800.2:p.Ser273Thr
XM_006721737.3:c.817T>A	XP_006721800.2:p.Ser273Thr
NM_000789.4:c.2479T>A MANE Select	NP_000780.1:p.Ser827Thr
NM_001178057.2:c.757T>A	NP_001171528.1:p.Ser253Thr
NM_152830.3:c.757T>A	NP_690043.1:p.Ser253Thr
NM_001382700.1:c.1912T>A	NP_001369629.1:p.Ser638Thr
NM_001382701.1:c.1627T>A	NP_001369630.1:p.Ser543Thr
NM_001382702.1:c.379+179T>A	NP_001369631.1:n.379+179T>A
NR_168483.1:n.857T>A