Canonical Allele Identifier: CA400567789

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574328A>C (hg19) ; chr17:g.63496967A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496967A>C , CM000679.2:g.63496967A>C	GRCh38
NC_000017.10:g.61574328A>C , CM000679.1:g.61574328A>C	GRCh37
NC_000017.9:g.58928060A>C	NCBI36
NG_011648.1:g.24895A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3673A>C MANE Select	ENSP00000290866.4:p.Asn1225His
ENST00000290863.10:c.1951A>C	ENSP00000290863.6:p.Asn651His
ENST00000290866.9:c.3673A>C	ENSP00000290866.4:p.Asn1225His
ENST00000413513.7:c.1828A>C	ENSP00000392247.3:p.Asn610His
ENST00000428043.5:c.3673A>C	ENSP00000397593.2:p.Asn1225His
ENST00000577418.5:n.683A>C
ENST00000577647.2:c.1951A>C	ENSP00000464149.1:p.Asn651His
ENST00000578839.5:c.*1428A>C	ENSP00000462110.2:n.*1428A>C
ENST00000579314.5:c.*1402A>C	ENSP00000462599.1:n.*1402A>C
ENST00000579409.1:c.360A>C
ENST00000582244.1:n.547A>C
NM_000789.3:c.3673A>C	NP_000780.1:p.Asn1225His
NM_001178057.1:c.1828A>C	NP_001171528.1:p.Asn610His
NM_152830.2:c.1951A>C	NP_690043.1:p.Asn651His
XM_005257110.1:c.3124A>C	XP_005257167.1:p.Asn1042His
XM_006721737.2:c.2011A>C	XP_006721800.2:p.Asn671His
XM_006721737.3:c.2011A>C	XP_006721800.2:p.Asn671His
NM_000789.4:c.3673A>C MANE Select	NP_000780.1:p.Asn1225His
NM_001178057.2:c.1828A>C	NP_001171528.1:p.Asn610His
NM_152830.3:c.1951A>C	NP_690043.1:p.Asn651His
NM_001382700.1:c.3106A>C	NP_001369629.1:p.Asn1036His
NM_001382701.1:c.2821A>C	NP_001369630.1:p.Asn941His
NM_001382702.1:c.1288A>C	NP_001369631.1:p.Asn430His
NR_168483.1:n.2051A>C