Canonical Allele Identifier: CA2269946068

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488932C= , CM000679.2:g.63488932C=	GRCh38
NC_000017.10:g.61566293C= , CM000679.1:g.61566293C=	GRCh37
NC_000017.9:g.58920025C=	NCBI36
NG_011648.1:g.16860C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2450-9C= MANE Select	ENSP00000290866.4:n.2450-9C=
ENST00000290863.10:c.728-9C=	ENSP00000290863.6:n.728-9C=
ENST00000290866.9:c.2450-9C=	ENSP00000290866.4:n.2450-9C=
ENST00000413513.7:c.728-9C=	ENSP00000392247.3:n.728-9C=
ENST00000428043.5:c.2450-9C=	ENSP00000397593.2:n.2450-9C=
ENST00000577647.2:c.728-9C=	ENSP00000464149.1:n.728-9C=
ENST00000578839.5:c.*519+141C=	ENSP00000462110.2:n.*519+141C=
ENST00000579204.1:c.709-9C=	ENSP00000464629.1:n.709-9C=
ENST00000579314.5:c.*179-9C=	ENSP00000462599.1:n.*179-9C=
ENST00000582005.5:c.*370-9C=	ENSP00000462002.1:n.*370-9C=
ENST00000582761.1:c.218-9C=	ENSP00000462909.1:n.218-9C=
ENST00000584865.5:n.396-9C=
NM_000789.3:c.2450-9C=	NP_000780.1:n.2450-9C=
NM_001178057.1:c.728-9C=	NP_001171528.1:n.728-9C=
NM_152830.2:c.728-9C=	NP_690043.1:n.728-9C=
XM_005257110.1:c.1901-9C=	XP_005257167.1:n.1901-9C=
XM_006721737.2:c.788-9C=	XP_006721800.2:n.788-9C=
XM_006721737.3:c.788-9C=	XP_006721800.2:n.788-9C=
NM_000789.4:c.2450-9C= MANE Select	NP_000780.1:n.2450-9C=
NM_001178057.2:c.728-9C=	NP_001171528.1:n.728-9C=
NM_152830.3:c.728-9C=	NP_690043.1:n.728-9C=
NM_001382700.1:c.1883-9C=	NP_001369629.1:n.1883-9C=
NM_001382701.1:c.1598-9C=	NP_001369630.1:n.1598-9C=
NM_001382702.1:c.379+141C=	NP_001369631.1:n.379+141C=
NR_168483.1:n.828-9C=