Canonical Allele Identifier: CA2269944988

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486878_63486886delinsAGCTCCCTG , CM000679.2:g.63486878_63486886delinsAGCTCCCTG	GRCh38
NC_000017.10:g.61564239_61564247delinsAGCTCCCTG , CM000679.1:g.61564239_61564247delinsAGCTCCCTG	GRCh37
NC_000017.9:g.58917971_58917979delinsAGCTCCCTG	NCBI36
NG_011648.1:g.14806_14814delinsAGCTCCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2218-108_2218-100delinsAGCTCCCTG MANE Select	ENSP00000290866.4:n.2218-108_2218-100delinsAGCTCCCTG
ENST00000290863.10:c.496-108_496-100delinsAGCTCCCTG	ENSP00000290863.6:n.496-108_496-100delinsAGCTCCCTG
ENST00000290866.9:c.2218-108_2218-100delinsAGCTCCCTG	ENSP00000290866.4:n.2218-108_2218-100delinsAGCTCCCTG
ENST00000413513.7:c.496-108_496-100delinsAGCTCCCTG	ENSP00000392247.3:n.496-108_496-100delinsAGCTCCCTG
ENST00000428043.5:c.2218-108_2218-100delinsAGCTCCCTG	ENSP00000397593.2:n.2218-108_2218-100delinsAGCTCCCTG
ENST00000577647.2:c.496-108_496-100delinsAGCTCCCTG	ENSP00000464149.1:n.496-108_496-100delinsAGCTCCCTG
ENST00000578839.5:c.*288-108_*288-100delinsAGCTCCCTG	ENSP00000462110.2:n.*288-108_*288-100delinsAGCTCCCTG
ENST00000579204.1:c.399-108_399-100delinsAGCTCCCTG	ENSP00000464629.1:n.399-108_399-100delinsAGCTCCCTG
ENST00000579314.5:c.496-108_496-100delinsAGCTCCCTG	ENSP00000462599.1:n.496-108_496-100delinsAGCTCCCTG
ENST00000579726.5:c.780-108_780-100delinsAGCTCCCTG
ENST00000582005.5:c.*138-108_*138-100delinsAGCTCCCTG	ENSP00000462002.1:n.*138-108_*138-100delinsAGCTCCCTG
ENST00000584865.5:n.56_64delinsAGCTCCCTG
NM_000789.3:c.2218-108_2218-100delinsAGCTCCCTG	NP_000780.1:n.2218-108_2218-100delinsAGCTCCCTG
NM_001178057.1:c.496-108_496-100delinsAGCTCCCTG	NP_001171528.1:n.496-108_496-100delinsAGCTCCCTG
NM_152830.2:c.496-108_496-100delinsAGCTCCCTG	NP_690043.1:n.496-108_496-100delinsAGCTCCCTG
XM_005257110.1:c.1669-108_1669-100delinsAGCTCCCTG	XP_005257167.1:n.1669-108_1669-100delinsAGCTCCCTG
XM_006721737.2:c.556-108_556-100delinsAGCTCCCTG	XP_006721800.2:n.556-108_556-100delinsAGCTCCCTG
XM_006721737.3:c.556-108_556-100delinsAGCTCCCTG	XP_006721800.2:n.556-108_556-100delinsAGCTCCCTG
NM_000789.4:c.2218-108_2218-100delinsAGCTCCCTG MANE Select	NP_000780.1:n.2218-108_2218-100delinsAGCTCCCTG
NM_001178057.2:c.496-108_496-100delinsAGCTCCCTG	NP_001171528.1:n.496-108_496-100delinsAGCTCCCTG
NM_152830.3:c.496-108_496-100delinsAGCTCCCTG	NP_690043.1:n.496-108_496-100delinsAGCTCCCTG
NM_001382700.1:c.1651-108_1651-100delinsAGCTCCCTG	NP_001369629.1:n.1651-108_1651-100delinsAGCTCCCTG
NM_001382701.1:c.1366-108_1366-100delinsAGCTCCCTG	NP_001369630.1:n.1366-108_1366-100delinsAGCTCCCTG
NM_001382702.1:c.148-108_148-100delinsAGCTCCCTG	NP_001369631.1:n.148-108_148-100delinsAGCTCCCTG
NR_168483.1:n.518-108_518-100delinsAGCTCCCTG