Canonical Allele Identifier: CA773975200

Gene: ACE

Linked Data

• dbSNP Id: rs1381402276
• MyVariant Identifiers: chr17:g.61575697_61575700del (hg19) ; chr17:g.63498336_63498339del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498336_63498339del , CM000679.2:g.63498336_63498339del	GRCh38
NC_000017.10:g.61575697_61575700del , CM000679.1:g.61575697_61575700del	GRCh37
NC_000017.9:g.58929429_58929432del	NCBI36
NG_011648.1:g.26264_26267del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*970_*973del MANE Select	ENSP00000290866.4:n.*970_*973del
ENST00000290866.9:c.*970_*973del	ENSP00000290866.4:n.*970_*973del
ENST00000428043.5:c.*1313_*1316del	ENSP00000397593.2:n.*1313_*1316del
ENST00000577647.2:c.1969+1351_1969+1354del	ENSP00000464149.1:n.1969+1351_1969+1354del
NM_000789.3:c.*970_*973del	NP_000780.1:n.*970_*973del
NM_001178057.1:c.*970_*973del	NP_001171528.1:n.*970_*973del
NM_152830.2:c.*970_*973del	NP_690043.1:n.*970_*973del
XM_005257110.1:c.*970_*973del	XP_005257167.1:n.*970_*973del
XM_006721737.2:c.*970_*973del	XP_006721800.2:n.*970_*973del
NM_000789.4:c.*970_*973del MANE Select	NP_000780.1:n.*970_*973del
NM_001178057.2:c.*970_*973del	NP_001171528.1:n.*970_*973del
NM_152830.3:c.*970_*973del	NP_690043.1:n.*970_*973del
NM_001382700.1:c.*970_*973del	NP_001369629.1:n.*970_*973del
NM_001382701.1:c.*970_*973del	NP_001369630.1:n.*970_*973del
NM_001382702.1:c.*970_*973del	NP_001369631.1:n.*970_*973del
NR_168483.1:n.3269_3272del