Canonical Allele Identifier: CA14383525

Gene: ACE

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63493061A>G , CM000679.2:g.63493061A>G	GRCh38
NC_000017.10:g.61570422A>G , CM000679.1:g.61570422A>G	GRCh37
NC_000017.9:g.58924154A>G	NCBI36
NG_011648.1:g.20989A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2913-375A>G MANE Select	ENSP00000290866.4:n.2913-375A>G
ENST00000290863.10:c.1191-375A>G	ENSP00000290863.6:n.1191-375A>G
ENST00000290866.9:c.2913-375A>G	ENSP00000290866.4:n.2913-375A>G
ENST00000413513.7:c.1191-375A>G	ENSP00000392247.3:n.1191-375A>G
ENST00000428043.5:c.2913-375A>G	ENSP00000397593.2:n.2913-375A>G
ENST00000577418.5:n.147-861A>G
ENST00000577647.2:c.1191-375A>G	ENSP00000464149.1:n.1191-375A>G
ENST00000578839.5:c.*791-375A>G	ENSP00000462110.2:n.*791-375A>G
ENST00000579314.5:c.*642-375A>G	ENSP00000462599.1:n.*642-375A>G
ENST00000582761.1:c.668-861A>G	ENSP00000462909.1:n.668-861A>G
ENST00000583645.1:n.878-375A>G
ENST00000584865.5:n.859-375A>G
NM_000789.3:c.2913-375A>G	NP_000780.1:n.2913-375A>G
NM_001178057.1:c.1191-375A>G	NP_001171528.1:n.1191-375A>G
NM_152830.2:c.1191-375A>G	NP_690043.1:n.1191-375A>G
XM_005257110.1:c.2364-375A>G	XP_005257167.1:n.2364-375A>G
XM_006721737.2:c.1251-375A>G	XP_006721800.2:n.1251-375A>G
XM_006721737.3:c.1251-375A>G	XP_006721800.2:n.1251-375A>G
NM_000789.4:c.2913-375A>G MANE Select	NP_000780.1:n.2913-375A>G
NM_001178057.2:c.1191-375A>G	NP_001171528.1:n.1191-375A>G
NM_152830.3:c.1191-375A>G	NP_690043.1:n.1191-375A>G
NM_001382700.1:c.2346-375A>G	NP_001369629.1:n.2346-375A>G
NM_001382701.1:c.2061-375A>G	NP_001369630.1:n.2061-375A>G
NM_001382702.1:c.651-375A>G	NP_001369631.1:n.651-375A>G
NR_168483.1:n.1291-375A>G