Canonical Allele Identifier: CA1619451826

Gene: AGER

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32182207C= , CM000668.2:g.32182207C=	GRCh38
NC_000006.11:g.32149984C= , CM000668.1:g.32149984C=	GRCh37
NC_000006.10:g.32257962C=	NCBI36
NG_029868.1:g.7116G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.964+40G= MANE Select	ENSP00000364217.4:n.964+40G=
ENST00000375055.6:c.964+40G=	ENSP00000364195.2:n.964+40G=
ENST00000375065.6:c.151+40G=	ENSP00000364206.6:n.151+40G=
ENST00000375067.7:c.809+332G=	ENSP00000364208.3:n.809+332G=
ENST00000375069.7:c.1012+40G=	ENSP00000364210.4:n.1012+40G=
ENST00000375070.7:c.661+40G=	ENSP00000364211.4:n.661+40G=
ENST00000375076.8:c.964+40G=	ENSP00000364217.4:n.964+40G=
ENST00000438221.6:c.1012+40G=	ENSP00000387887.2:n.1012+40G=
ENST00000473619.5:n.506+40G=
ENST00000484849.5:n.1171+40G=
ENST00000488669.5:n.506+40G=
ENST00000620802.4:c.283-774G=	ENSP00000484081.1:n.283-774G=
NM_001136.4:c.964+40G=	NP_001127.1:n.964+40G=
NM_001206929.1:c.1012+40G=	NP_001193858.1:n.1012+40G=
NM_001206932.1:c.922+40G=	NP_001193861.1:n.922+40G=
NM_001206934.1:c.1012+40G=	NP_001193863.1:n.1012+40G=
NM_001206936.1:c.912+40G=	NP_001193865.1:n.912+40G=
NM_001206940.1:c.964+40G=	NP_001193869.1:n.964+40G=
NM_001206954.1:c.822+361G=	NP_001193883.1:n.822+361G=
NM_001206966.1:c.964+40G=	NP_001193895.1:n.964+40G=
NM_172197.2:c.809+332G=	NP_751947.1:n.809+332G=
NR_038190.1:n.1247+40G=
XM_017010328.2:c.963+361G=	XP_016865817.1:n.963+361G=
XR_001743189.2:n.1028+361G=
XR_001743190.2:n.980+361G=
NM_001136.5:c.964+40G= MANE Select	NP_001127.1:n.964+40G=
NM_001206932.2:c.922+40G=	NP_001193861.1:n.922+40G=
NM_001206936.2:c.912+40G=	NP_001193865.1:n.912+40G=
NM_001206940.2:c.964+40G=	NP_001193869.1:n.964+40G=
NM_001206954.2:c.822+361G=	NP_001193883.1:n.822+361G=
NM_001206966.2:c.964+40G=	NP_001193895.1:n.964+40G=
NM_172197.3:c.809+332G=	NP_751947.1:n.809+332G=
NR_038190.2:n.1178+40G=
NM_001206929.2:c.1012+40G=	NP_001193858.1:n.1012+40G=
NM_001206934.2:c.1012+40G=	NP_001193863.1:n.1012+40G=