Canonical Allele Identifier: CA773960792

Gene: ACE

Linked Data

• dbSNP Id: rs1474182198
• MyVariant Identifiers: chr17:g.61558185_61558186del (hg19) ; chr17:g.63480824_63480825del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63480824_63480825del , CM000679.2:g.63480824_63480825del	GRCh38
NC_000017.10:g.61558185_61558186del , CM000679.1:g.61558185_61558186del	GRCh37
NC_000017.9:g.58911917_58911918del	NCBI36
NG_011648.1:g.8752_8753del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.848-267_848-266del MANE Select	ENSP00000290866.4:n.848-267_848-266del
ENST00000290866.9:c.848-267_848-266del	ENSP00000290866.4:n.848-267_848-266del
ENST00000428043.5:c.848-267_848-266del	ENSP00000397593.2:n.848-267_848-266del
ENST00000582627.1:c.848-267_848-266del	ENSP00000462280.1:n.848-267_848-266del
ENST00000582678.5:c.*247-267_*247-266del	ENSP00000462995.1:n.*247-267_*247-266del
ENST00000584529.5:n.882-267_882-266del
NM_000789.3:c.848-267_848-266del	NP_000780.1:n.848-267_848-266del
XM_005257110.1:c.299-267_299-266del	XP_005257167.1:n.299-267_299-266del
NM_000789.4:c.848-267_848-266del MANE Select	NP_000780.1:n.848-267_848-266del
NM_001382700.1:c.375-267_375-266del	NP_001369629.1:n.375-267_375-266del
NM_001382701.1:c.-5-267_-5-266del	NP_001369630.1:n.-5-267_-5-266del