Canonical Allele Identifier: CA2639236808

Gene: ACE

Linked Data

• gnomAD v4: 17-63477142-G-GCCGCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477147_63477148insTCCGCT , CM000679.2:g.63477147_63477148insTCCGCT	GRCh38
NC_000017.10:g.61554508_61554509insTCCGCT , CM000679.1:g.61554508_61554509insTCCGCT	GRCh37
NC_000017.9:g.58908240_58908241insTCCGCT	NCBI36
NG_011648.1:g.5075_5076insTCCGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.53_54insTCCGCT MANE Select	ENSP00000290866.4:p.Leu18_Leu19insProLeu
ENST00000290866.9:c.53_54insTCCGCT	ENSP00000290866.4:p.Leu18_Leu19insProLeu
ENST00000428043.5:c.53_54insTCCGCT	ENSP00000397593.2:p.Leu18_Leu19insProLeu
ENST00000579462.1:n.78_79insTCCGCT
ENST00000582678.5:c.53_54insTCCGCT	ENSP00000462995.1:p.Leu18_Leu19insProLeu
ENST00000583336.5:n.87_88insTCCGCT
ENST00000584529.5:n.87_88insTCCGCT
NM_000789.3:c.53_54insTCCGCT	NP_000780.1:p.Leu18_Leu19insProLeu
XM_005257110.1:c.-403_-402insTCCGCT	XP_005257167.1:n.-403_-402insTCCGCT
NM_000789.4:c.53_54insTCCGCT MANE Select	NP_000780.1:p.Leu18_Leu19insProLeu
NM_001382700.1:c.-183_-182insTCCGCT	NP_001369629.1:n.-183_-182insTCCGCT
NM_001382701.1:c.-562_-561insTCCGCT	NP_001369630.1:n.-562_-561insTCCGCT