Canonical Allele Identifier: CA2269950438

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497959_63497970delinsGGGGAAGGCTTC , CM000679.2:g.63497959_63497970delinsGGGGAAGGCTTC	GRCh38
NC_000017.10:g.61575320_61575331delinsGGGGAAGGCTTC , CM000679.1:g.61575320_61575331delinsGGGGAAGGCTTC	GRCh37
NC_000017.9:g.58929052_58929063delinsGGGGAAGGCTTC	NCBI36
NG_011648.1:g.25887_25898delinsGGGGAAGGCTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*593_*604delinsGGGGAAGGCTTC MANE Select	ENSP00000290866.4:n.*593_*604delinsGGGGAAGGCTTC
ENST00000290866.9:c.*593_*604delinsGGGGAAGGCTTC	ENSP00000290866.4:n.*593_*604delinsGGGGAAGGCTTC
ENST00000428043.5:c.*936_*947delinsGGGGAAGGCTTC	ENSP00000397593.2:n.*936_*947delinsGGGGAAGGCTTC
ENST00000577647.2:c.1969+974_1969+985delinsGGGGAAGGCTTC	ENSP00000464149.1:n.1969+974_1969+985delinsGGGGAAGGCTTC
NM_000789.3:c.*593_*604delinsGGGGAAGGCTTC	NP_000780.1:n.*593_*604delinsGGGGAAGGCTTC
NM_001178057.1:c.*593_*604delinsGGGGAAGGCTTC	NP_001171528.1:n.*593_*604delinsGGGGAAGGCTTC
NM_152830.2:c.*593_*604delinsGGGGAAGGCTTC	NP_690043.1:n.*593_*604delinsGGGGAAGGCTTC
XM_005257110.1:c.*593_*604delinsGGGGAAGGCTTC	XP_005257167.1:n.*593_*604delinsGGGGAAGGCTTC
XM_006721737.2:c.*593_*604delinsGGGGAAGGCTTC	XP_006721800.2:n.*593_*604delinsGGGGAAGGCTTC
NM_000789.4:c.*593_*604delinsGGGGAAGGCTTC MANE Select	NP_000780.1:n.*593_*604delinsGGGGAAGGCTTC
NM_001178057.2:c.*593_*604delinsGGGGAAGGCTTC	NP_001171528.1:n.*593_*604delinsGGGGAAGGCTTC
NM_152830.3:c.*593_*604delinsGGGGAAGGCTTC	NP_690043.1:n.*593_*604delinsGGGGAAGGCTTC
NM_001382700.1:c.*593_*604delinsGGGGAAGGCTTC	NP_001369629.1:n.*593_*604delinsGGGGAAGGCTTC
NM_001382701.1:c.*593_*604delinsGGGGAAGGCTTC	NP_001369630.1:n.*593_*604delinsGGGGAAGGCTTC
NM_001382702.1:c.*593_*604delinsGGGGAAGGCTTC	NP_001369631.1:n.*593_*604delinsGGGGAAGGCTTC
NR_168483.1:n.2892_2903delinsGGGGAAGGCTTC