Canonical Allele Identifier: CA400557980

Gene: ACE

Linked Data

• dbSNP Id: rs1568043111
• MyVariant Identifiers: chr17:g.61566101C>T (hg19) ; chr17:g.63488740C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488740C>T , CM000679.2:g.63488740C>T	GRCh38
NC_000017.10:g.61566101C>T , CM000679.1:g.61566101C>T	GRCh37
NC_000017.9:g.58919833C>T	NCBI36
NG_011648.1:g.16668C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2398C>T MANE Select	ENSP00000290866.4:p.Gln800Ter
ENST00000290863.10:c.676C>T	ENSP00000290863.6:p.Gln226Ter
ENST00000290866.9:c.2398C>T	ENSP00000290866.4:p.Gln800Ter
ENST00000413513.7:c.676C>T	ENSP00000392247.3:p.Gln226Ter
ENST00000428043.5:c.2398C>T	ENSP00000397593.2:p.Gln800Ter
ENST00000577647.2:c.676C>T	ENSP00000464149.1:p.Gln226Ter
ENST00000578839.5:c.*468C>T	ENSP00000462110.2:n.*468C>T
ENST00000579204.1:c.657C>T	ENSP00000464629.1:n.657C>T
ENST00000579314.5:c.*127C>T	ENSP00000462599.1:n.*127C>T
ENST00000582005.5:c.*318C>T	ENSP00000462002.1:n.*318C>T
ENST00000582761.1:c.166C>T	ENSP00000462909.1:p.Gln56Ter
ENST00000584865.5:n.344C>T
NM_000789.3:c.2398C>T	NP_000780.1:p.Gln800Ter
NM_001178057.1:c.676C>T	NP_001171528.1:p.Gln226Ter
NM_152830.2:c.676C>T	NP_690043.1:p.Gln226Ter
XM_005257110.1:c.1849C>T	XP_005257167.1:p.Gln617Ter
XM_006721737.2:c.736C>T	XP_006721800.2:p.Gln246Ter
XM_006721737.3:c.736C>T	XP_006721800.2:p.Gln246Ter
NM_000789.4:c.2398C>T MANE Select	NP_000780.1:p.Gln800Ter
NM_001178057.2:c.676C>T	NP_001171528.1:p.Gln226Ter
NM_152830.3:c.676C>T	NP_690043.1:p.Gln226Ter
NM_001382700.1:c.1831C>T	NP_001369629.1:p.Gln611Ter
NM_001382701.1:c.1546C>T	NP_001369630.1:p.Gln516Ter
NM_001382702.1:c.328C>T	NP_001369631.1:p.Gln110Ter
NR_168483.1:n.776C>T