Canonical Allele Identifier: CA400567712

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574317G>C (hg19) ; chr17:g.63496956G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496956G>C , CM000679.2:g.63496956G>C	GRCh38
NC_000017.10:g.61574317G>C , CM000679.1:g.61574317G>C	GRCh37
NC_000017.9:g.58928049G>C	NCBI36
NG_011648.1:g.24884G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3662G>C MANE Select	ENSP00000290866.4:p.Trp1221Ser
ENST00000290863.10:c.1940G>C	ENSP00000290863.6:p.Trp647Ser
ENST00000290866.9:c.3662G>C	ENSP00000290866.4:p.Trp1221Ser
ENST00000413513.7:c.1817G>C	ENSP00000392247.3:p.Trp606Ser
ENST00000428043.5:c.3662G>C	ENSP00000397593.2:p.Trp1221Ser
ENST00000577418.5:n.672G>C
ENST00000577647.2:c.1940G>C	ENSP00000464149.1:p.Trp647Ser
ENST00000578839.5:c.*1417G>C	ENSP00000462110.2:n.*1417G>C
ENST00000579314.5:c.*1391G>C	ENSP00000462599.1:n.*1391G>C
ENST00000579409.1:c.349G>C
ENST00000582244.1:n.536G>C
NM_000789.3:c.3662G>C	NP_000780.1:p.Trp1221Ser
NM_001178057.1:c.1817G>C	NP_001171528.1:p.Trp606Ser
NM_152830.2:c.1940G>C	NP_690043.1:p.Trp647Ser
XM_005257110.1:c.3113G>C	XP_005257167.1:p.Trp1038Ser
XM_006721737.2:c.2000G>C	XP_006721800.2:p.Trp667Ser
XM_006721737.3:c.2000G>C	XP_006721800.2:p.Trp667Ser
NM_000789.4:c.3662G>C MANE Select	NP_000780.1:p.Trp1221Ser
NM_001178057.2:c.1817G>C	NP_001171528.1:p.Trp606Ser
NM_152830.3:c.1940G>C	NP_690043.1:p.Trp647Ser
NM_001382700.1:c.3095G>C	NP_001369629.1:p.Trp1032Ser
NM_001382701.1:c.2810G>C	NP_001369630.1:p.Trp937Ser
NM_001382702.1:c.1277G>C	NP_001369631.1:p.Trp426Ser
NR_168483.1:n.2040G>C