Canonical Allele Identifier: CA1619451280

Gene: AGER

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32181373G= , CM000668.2:g.32181373G=	GRCh38
NC_000006.11:g.32149150G= , CM000668.1:g.32149150G=	GRCh37
NC_000006.10:g.32257128G=	NCBI36
NG_029868.1:g.7950C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.1096C= MANE Select	ENSP00000364217.4:p.Arg366=
ENST00000375055.6:c.*30-134C=	ENSP00000364195.2:n.*30-134C=
ENST00000375065.6:c.283C=	ENSP00000364206.6:p.Arg95=
ENST00000375067.7:c.941C=	ENSP00000364208.3:p.Ala314=
ENST00000375069.7:c.1144C=	ENSP00000364210.4:p.Arg382=
ENST00000375070.7:c.766C=	ENSP00000364211.4:p.Arg256=
ENST00000375076.8:c.1096C=	ENSP00000364217.4:p.Arg366=
ENST00000438221.6:c.*30-134C=	ENSP00000387887.2:n.*30-134C=
ENST00000469940.5:n.263C=
ENST00000473619.5:n.638C=
ENST00000484849.5:n.1303C=
ENST00000488669.5:n.616-134C=
ENST00000620802.4:c.343C=	ENSP00000484081.1:p.Arg115=
NM_001136.4:c.1096C=	NP_001127.1:p.Arg366=
NM_001206929.1:c.1144C=	NP_001193858.1:p.Arg382=
NM_001206932.1:c.1054C=	NP_001193861.1:p.Arg352=
NM_001206934.1:c.*30-134C=	NP_001193863.1:n.*30-134C=
NM_001206936.1:c.1022-134C=	NP_001193865.1:n.1022-134C=
NM_001206940.1:c.*30-134C=	NP_001193869.1:n.*30-134C=
NM_001206954.1:c.932-134C=	NP_001193883.1:n.932-134C=
NM_001206966.1:c.*29+151C=	NP_001193895.1:n.*29+151C=
NM_172197.2:c.941C=	NP_751947.1:p.Ala314=
NR_038190.1:n.1379C=
XM_017010328.2:c.1073-134C=	XP_016865817.1:n.1073-134C=
XR_001743189.2:n.1160C=
XR_001743190.2:n.1112C=
NM_001136.5:c.1096C= MANE Select	NP_001127.1:p.Arg366=
NM_001206932.2:c.1054C=	NP_001193861.1:p.Arg352=
NM_001206936.2:c.1022-134C=	NP_001193865.1:n.1022-134C=
NM_001206940.2:c.*30-134C=	NP_001193869.1:n.*30-134C=
NM_001206954.2:c.932-134C=	NP_001193883.1:n.932-134C=
NM_001206966.2:c.*29+151C=	NP_001193895.1:n.*29+151C=
NM_172197.3:c.941C=	NP_751947.1:p.Ala314=
NR_038190.2:n.1310C=
NM_001206929.2:c.1144C=	NP_001193858.1:p.Arg382=
NM_001206934.2:c.*30-134C=	NP_001193863.1:n.*30-134C=