Canonical Allele Identifier: CA1619451859

Gene: AGER

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32182249A= , CM000668.2:g.32182249A=	GRCh38
NC_000006.11:g.32150026A= , CM000668.1:g.32150026A=	GRCh37
NC_000006.10:g.32258004A=	NCBI36
NG_029868.1:g.7074T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.962T= MANE Select	ENSP00000364217.4:p.Ile321=
ENST00000375055.6:c.962T=	ENSP00000364195.2:p.Ile321=
ENST00000375065.6:c.149T=	ENSP00000364206.6:p.Ile50=
ENST00000375067.7:c.809+290T=	ENSP00000364208.3:n.809+290T=
ENST00000375069.7:c.1010T=	ENSP00000364210.4:p.Ile337=
ENST00000375070.7:c.659T=	ENSP00000364211.4:p.Ile220=
ENST00000375076.8:c.962T=	ENSP00000364217.4:p.Ile321=
ENST00000438221.6:c.1010T=	ENSP00000387887.2:p.Ile337=
ENST00000473619.5:n.504T=
ENST00000484849.5:n.1169T=
ENST00000488669.5:n.504T=
ENST00000620802.4:c.283-816T=	ENSP00000484081.1:n.283-816T=
NM_001136.4:c.962T=	NP_001127.1:p.Ile321=
NM_001206929.1:c.1010T=	NP_001193858.1:p.Ile337=
NM_001206932.1:c.920T=	NP_001193861.1:p.Ile307=
NM_001206934.1:c.1010T=	NP_001193863.1:p.Ile337=
NM_001206936.1:c.910T=	NP_001193865.1:p.Ser304=
NM_001206940.1:c.962T=	NP_001193869.1:p.Ile321=
NM_001206954.1:c.822+319T=	NP_001193883.1:n.822+319T=
NM_001206966.1:c.962T=	NP_001193895.1:p.Ile321=
NM_172197.2:c.809+290T=	NP_751947.1:n.809+290T=
NR_038190.1:n.1245T=
XM_017010328.2:c.963+319T=	XP_016865817.1:n.963+319T=
XR_001743189.2:n.1028+319T=
XR_001743190.2:n.980+319T=
NM_001136.5:c.962T= MANE Select	NP_001127.1:p.Ile321=
NM_001206932.2:c.920T=	NP_001193861.1:p.Ile307=
NM_001206936.2:c.910T=	NP_001193865.1:p.Ser304=
NM_001206940.2:c.962T=	NP_001193869.1:p.Ile321=
NM_001206954.2:c.822+319T=	NP_001193883.1:n.822+319T=
NM_001206966.2:c.962T=	NP_001193895.1:p.Ile321=
NM_172197.3:c.809+290T=	NP_751947.1:n.809+290T=
NR_038190.2:n.1176T=
NM_001206929.2:c.1010T=	NP_001193858.1:p.Ile337=
NM_001206934.2:c.1010T=	NP_001193863.1:p.Ile337=