Canonical Allele Identifier: CA773988013

Gene: ACE

Linked Data

• dbSNP Id: rs1321632628
• MyVariant Identifiers: chr17:g.61554515_61554523del (hg19) ; chr17:g.63477154_63477162del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477156_63477164del , CM000679.2:g.63477156_63477164del	GRCh38
NC_000017.10:g.61554517_61554525del , CM000679.1:g.61554517_61554525del	GRCh37
NC_000017.9:g.58908249_58908257del	NCBI36
NG_011648.1:g.5084_5092del

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.62_70del MANE Select	ENSP00000290866.4:p.Leu21_Pro23del
ENST00000290866.9:c.62_70del	ENSP00000290866.4:p.Leu21_Pro23del
ENST00000428043.5:c.62_70del	ENSP00000397593.2:p.Leu21_Pro23del
ENST00000579462.1:n.87_95del
ENST00000582678.5:c.62_70del	ENSP00000462995.1:p.Leu21_Pro23del
ENST00000583336.5:n.96_104del
ENST00000584529.5:n.96_104del
NM_000789.3:c.62_70del	NP_000780.1:p.Leu21_Pro23del
XM_005257110.1:c.-394_-386del	XP_005257167.1:n.-394_-386del
NM_000789.4:c.62_70del MANE Select	NP_000780.1:p.Leu21_Pro23del
NM_001382700.1:c.-174_-166del	NP_001369629.1:n.-174_-166del
NM_001382701.1:c.-553_-545del	NP_001369630.1:n.-553_-545del