Canonical Allele Identifier: CA2639245838

Gene: ACE

Linked Data

• gnomAD v4: 17-63498095-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498096_63498097insCC , CM000679.2:g.63498096_63498097insCC	GRCh38
NC_000017.10:g.61575457_61575458insCC , CM000679.1:g.61575457_61575458insCC	GRCh37
NC_000017.9:g.58929189_58929190insCC	NCBI36
NG_011648.1:g.26024_26025insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*730_*731insCC MANE Select	ENSP00000290866.4:n.*730_*731insCC
ENST00000290866.9:c.*730_*731insCC	ENSP00000290866.4:n.*730_*731insCC
ENST00000428043.5:c.*1073_*1074insCC	ENSP00000397593.2:n.*1073_*1074insCC
ENST00000577647.2:c.1969+1111_1969+1112insCC	ENSP00000464149.1:n.1969+1111_1969+1112insCC
NM_000789.3:c.*730_*731insCC	NP_000780.1:n.*730_*731insCC
NM_001178057.1:c.*730_*731insCC	NP_001171528.1:n.*730_*731insCC
NM_152830.2:c.*730_*731insCC	NP_690043.1:n.*730_*731insCC
XM_005257110.1:c.*730_*731insCC	XP_005257167.1:n.*730_*731insCC
XM_006721737.2:c.*730_*731insCC	XP_006721800.2:n.*730_*731insCC
NM_000789.4:c.*730_*731insCC MANE Select	NP_000780.1:n.*730_*731insCC
NM_001178057.2:c.*730_*731insCC	NP_001171528.1:n.*730_*731insCC
NM_152830.3:c.*730_*731insCC	NP_690043.1:n.*730_*731insCC
NM_001382700.1:c.*730_*731insCC	NP_001369629.1:n.*730_*731insCC
NM_001382701.1:c.*730_*731insCC	NP_001369630.1:n.*730_*731insCC
NM_001382702.1:c.*730_*731insCC	NP_001369631.1:n.*730_*731insCC
NR_168483.1:n.3029_3030insCC