Canonical Allele Identifier: CA2269949831

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496957G= , CM000679.2:g.63496957G=	GRCh38
NC_000017.10:g.61574318G= , CM000679.1:g.61574318G=	GRCh37
NC_000017.9:g.58928050G=	NCBI36
NG_011648.1:g.24885G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3663G= MANE Select	ENSP00000290866.4:p.Trp1221=
ENST00000290863.10:c.1941G=	ENSP00000290863.6:p.Trp647=
ENST00000290866.9:c.3663G=	ENSP00000290866.4:p.Trp1221=
ENST00000413513.7:c.1818G=	ENSP00000392247.3:p.Trp606=
ENST00000428043.5:c.3663G=	ENSP00000397593.2:p.Trp1221=
ENST00000577418.5:n.673G=
ENST00000577647.2:c.1941G=	ENSP00000464149.1:p.Trp647=
ENST00000578839.5:c.*1418G=	ENSP00000462110.2:n.*1418G=
ENST00000579314.5:c.*1392G=	ENSP00000462599.1:n.*1392G=
ENST00000579409.1:c.350G=
ENST00000582244.1:n.537G=
NM_000789.3:c.3663G=	NP_000780.1:p.Trp1221=
NM_001178057.1:c.1818G=	NP_001171528.1:p.Trp606=
NM_152830.2:c.1941G=	NP_690043.1:p.Trp647=
XM_005257110.1:c.3114G=	XP_005257167.1:p.Trp1038=
XM_006721737.2:c.2001G=	XP_006721800.2:p.Trp667=
XM_006721737.3:c.2001G=	XP_006721800.2:p.Trp667=
NM_000789.4:c.3663G= MANE Select	NP_000780.1:p.Trp1221=
NM_001178057.2:c.1818G=	NP_001171528.1:p.Trp606=
NM_152830.3:c.1941G=	NP_690043.1:p.Trp647=
NM_001382700.1:c.3096G=	NP_001369629.1:p.Trp1032=
NM_001382701.1:c.2811G=	NP_001369630.1:p.Trp937=
NM_001382702.1:c.1278G=	NP_001369631.1:p.Trp426=
NR_168483.1:n.2041G=