Canonical Allele Identifier: CA2810114346

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486691_63486870del , CM000679.2:g.63486691_63486870del	GRCh38
NC_000017.10:g.61564052_61564231del , CM000679.1:g.61564052_61564231del	GRCh37
NC_000017.9:g.58917784_58917963del	NCBI36
NG_011648.1:g.14619_14798del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2193_2218-116del
ENST00000290863.10:c.471_496-116del
ENST00000290866.9:c.2193_2218-116del
ENST00000413513.7:c.471_496-116del
ENST00000428043.5:c.2193_2218-116del
ENST00000577647.2:c.471_496-116del
ENST00000578839.5:c.*263_*288-116del
ENST00000579204.1:c.374_399-116del
ENST00000579314.5:c.471_496-116del
ENST00000579726.5:c.755_780-116del
ENST00000582005.5:c.*113_*138-116del
NM_000789.3:c.2193_2218-116del
NM_001178057.1:c.471_496-116del
NM_152830.2:c.471_496-116del
XM_005257110.1:c.1644_1669-116del
XM_006721737.2:c.531_556-116del
XM_006721737.3:c.531_556-116del
NM_000789.4:c.2193_2218-116del
NM_001178057.2:c.471_496-116del
NM_152830.3:c.471_496-116del
NM_001382700.1:c.1626_1651-116del
NM_001382701.1:c.1341_1366-116del
NM_001382702.1:c.123_148-116del
NR_168483.1:n.493_518-116del