Canonical Allele Identifier: CA1619451456

Gene: AGER

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32181622C= , CM000668.2:g.32181622C=	GRCh38
NC_000006.11:g.32149399C= , CM000668.1:g.32149399C=	GRCh37
NC_000006.10:g.32257377C=	NCBI36
NG_029868.1:g.7701G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.975G= MANE Select	ENSP00000364217.4:p.Glu325=
ENST00000375055.6:c.975G=	ENSP00000364195.2:p.Glu325=
ENST00000375065.6:c.162G=	ENSP00000364206.6:p.Glu54=
ENST00000375067.7:c.820G=	ENSP00000364208.3:p.Gly274=
ENST00000375069.7:c.1023G=	ENSP00000364210.4:p.Glu341=
ENST00000375070.7:c.662-145G=	ENSP00000364211.4:n.662-145G=
ENST00000375076.8:c.975G=	ENSP00000364217.4:p.Glu325=
ENST00000438221.6:c.1023G=	ENSP00000387887.2:p.Glu341=
ENST00000469940.5:n.14G=
ENST00000473619.5:n.517G=
ENST00000484849.5:n.1182G=
ENST00000488669.5:n.517G=
ENST00000620802.4:c.283-189G=	ENSP00000484081.1:n.283-189G=
NM_001136.4:c.975G=	NP_001127.1:p.Glu325=
NM_001206929.1:c.1023G=	NP_001193858.1:p.Glu341=
NM_001206932.1:c.933G=	NP_001193861.1:p.Glu311=
NM_001206934.1:c.1023G=	NP_001193863.1:p.Glu341=
NM_001206936.1:c.923G=	NP_001193865.1:p.Arg308=
NM_001206940.1:c.975G=	NP_001193869.1:p.Glu325=
NM_001206954.1:c.833G=	NP_001193883.1:p.Arg278=
NM_001206966.1:c.975G=	NP_001193895.1:p.Glu325=
NM_172197.2:c.820G=	NP_751947.1:p.Gly274=
NR_038190.1:n.1258G=
XM_017010328.2:c.974G=	XP_016865817.1:p.Arg325=
XR_001743189.2:n.1039G=
XR_001743190.2:n.991G=
NM_001136.5:c.975G= MANE Select	NP_001127.1:p.Glu325=
NM_001206932.2:c.933G=	NP_001193861.1:p.Glu311=
NM_001206936.2:c.923G=	NP_001193865.1:p.Arg308=
NM_001206940.2:c.975G=	NP_001193869.1:p.Glu325=
NM_001206954.2:c.833G=	NP_001193883.1:p.Arg278=
NM_001206966.2:c.975G=	NP_001193895.1:p.Glu325=
NM_172197.3:c.820G=	NP_751947.1:p.Gly274=
NR_038190.2:n.1189G=
NM_001206929.2:c.1023G=	NP_001193858.1:p.Glu341=
NM_001206934.2:c.1023G=	NP_001193863.1:p.Glu341=