Canonical Allele Identifier: CA2639242332

Gene: ACE

Linked Data

• gnomAD v4: 17-63496771-C-CTGCCTCCCTGTCTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496780_63496794dup , CM000679.2:g.63496780_63496794dup	GRCh38
NC_000017.10:g.61574141_61574155dup , CM000679.1:g.61574141_61574155dup	GRCh37
NC_000017.9:g.58927873_58927887dup	NCBI36
NG_011648.1:g.24708_24722dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3504-18_3504-4dup MANE Select	ENSP00000290866.4:n.3504-18_3504-4dup
ENST00000290863.10:c.1782-18_1782-4dup	ENSP00000290863.6:n.1782-18_1782-4dup
ENST00000290866.9:c.3504-18_3504-4dup	ENSP00000290866.4:n.3504-18_3504-4dup
ENST00000413513.7:c.1659-18_1659-4dup	ENSP00000392247.3:n.1659-18_1659-4dup
ENST00000428043.5:c.3504-18_3504-4dup	ENSP00000397593.2:n.3504-18_3504-4dup
ENST00000577418.5:n.514-18_514-4dup
ENST00000577647.2:c.1782-18_1782-4dup	ENSP00000464149.1:n.1782-18_1782-4dup
ENST00000578839.5:c.*1259-18_*1259-4dup	ENSP00000462110.2:n.*1259-18_*1259-4dup
ENST00000579314.5:c.*1233-18_*1233-4dup	ENSP00000462599.1:n.*1233-18_*1233-4dup
ENST00000579409.1:c.191-18_191-4dup
ENST00000582244.1:n.378-18_378-4dup
NM_000789.3:c.3504-18_3504-4dup	NP_000780.1:n.3504-18_3504-4dup
NM_001178057.1:c.1659-18_1659-4dup	NP_001171528.1:n.1659-18_1659-4dup
NM_152830.2:c.1782-18_1782-4dup	NP_690043.1:n.1782-18_1782-4dup
XM_005257110.1:c.2955-18_2955-4dup	XP_005257167.1:n.2955-18_2955-4dup
XM_006721737.2:c.1842-18_1842-4dup	XP_006721800.2:n.1842-18_1842-4dup
XM_006721737.3:c.1842-18_1842-4dup	XP_006721800.2:n.1842-18_1842-4dup
NM_000789.4:c.3504-18_3504-4dup MANE Select	NP_000780.1:n.3504-18_3504-4dup
NM_001178057.2:c.1659-18_1659-4dup	NP_001171528.1:n.1659-18_1659-4dup
NM_152830.3:c.1782-18_1782-4dup	NP_690043.1:n.1782-18_1782-4dup
NM_001382700.1:c.2937-18_2937-4dup	NP_001369629.1:n.2937-18_2937-4dup
NM_001382701.1:c.2652-18_2652-4dup	NP_001369630.1:n.2652-18_2652-4dup
NM_001382702.1:c.1119-18_1119-4dup	NP_001369631.1:n.1119-18_1119-4dup
NR_168483.1:n.1882-18_1882-4dup