Canonical Allele Identifier: CA292874250
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs1023235603
MyVariant Identifiers: chr17:g.61558240T>A (hg19) chr17:g.63480879T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63480879T>A , CM000679.2:g.63480879T>A GRCh38
NC_000017.10:g.61558240T>A , CM000679.1:g.61558240T>A GRCh37
NC_000017.9:g.58911972T>A NCBI36
NG_011648.1:g.8807T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000290866.10:c.848-212T>A MANE Select ENSP00000290866.4:n.848-212T>A
ENST00000290866.9:c.848-212T>A ENSP00000290866.4:n.848-212T>A
ENST00000428043.5:c.848-212T>A ENSP00000397593.2:n.848-212T>A
ENST00000582627.1:c.848-212T>A ENSP00000462280.1:n.848-212T>A
ENST00000582678.5:c.*247-212T>A ENSP00000462995.1:n.*247-212T>A
ENST00000584529.5:n.882-212T>A
NM_000789.3:c.848-212T>A NP_000780.1:n.848-212T>A
XM_005257110.1:c.299-212T>A XP_005257167.1:n.299-212T>A
NM_000789.4:c.848-212T>A MANE Select NP_000780.1:n.848-212T>A
NM_001382700.1:c.375-212T>A NP_001369629.1:n.375-212T>A
NM_001382701.1:c.-5-212T>A NP_001369630.1:n.-5-212T>A
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