Canonical Allele Identifier: CA1619451401

Gene: AGER

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32181547C= , CM000668.2:g.32181547C=	GRCh38
NC_000006.11:g.32149324C= , CM000668.1:g.32149324C=	GRCh37
NC_000006.10:g.32257302C=	NCBI36
NG_029868.1:g.7776G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375076.9:c.991+59G= MANE Select	ENSP00000364217.4:n.991+59G=
ENST00000375055.6:c.*6G=	ENSP00000364195.2:n.*6G=
ENST00000375065.6:c.178+59G=	ENSP00000364206.6:n.178+59G=
ENST00000375067.7:c.836+59G=	ENSP00000364208.3:n.836+59G=
ENST00000375069.7:c.1039+59G=	ENSP00000364210.4:n.1039+59G=
ENST00000375070.7:c.662-70G=	ENSP00000364211.4:n.662-70G=
ENST00000375076.8:c.991+59G=	ENSP00000364217.4:n.991+59G=
ENST00000438221.6:c.*6G=	ENSP00000387887.2:n.*6G=
ENST00000469940.5:n.89G=
ENST00000473619.5:n.533+59G=
ENST00000484849.5:n.1198+59G=
ENST00000488669.5:n.592G=
ENST00000620802.4:c.283-114G=	ENSP00000484081.1:n.283-114G=
NM_001136.4:c.991+59G=	NP_001127.1:n.991+59G=
NM_001206929.1:c.1039+59G=	NP_001193858.1:n.1039+59G=
NM_001206932.1:c.949+59G=	NP_001193861.1:n.949+59G=
NM_001206934.1:c.*6G=	NP_001193863.1:n.*6G=
NM_001206936.1:c.998G=	NP_001193865.1:p.Gly333=
NM_001206940.1:c.*6G=	NP_001193869.1:n.*6G=
NM_001206954.1:c.908G=	NP_001193883.1:p.Gly303=
NM_001206966.1:c.*6G=	NP_001193895.1:n.*6G=
NM_172197.2:c.836+59G=	NP_751947.1:n.836+59G=
NR_038190.1:n.1274+59G=
XM_017010328.2:c.1049G=	XP_016865817.1:p.Gly350=
XR_001743189.2:n.1055+59G=
XR_001743190.2:n.1007+59G=
NM_001136.5:c.991+59G= MANE Select	NP_001127.1:n.991+59G=
NM_001206932.2:c.949+59G=	NP_001193861.1:n.949+59G=
NM_001206936.2:c.998G=	NP_001193865.1:p.Gly333=
NM_001206940.2:c.*6G=	NP_001193869.1:n.*6G=
NM_001206954.2:c.908G=	NP_001193883.1:p.Gly303=
NM_001206966.2:c.*6G=	NP_001193895.1:n.*6G=
NM_172197.3:c.836+59G=	NP_751947.1:n.836+59G=
NR_038190.2:n.1205+59G=
NM_001206929.2:c.1039+59G=	NP_001193858.1:n.1039+59G=
NM_001206934.2:c.*6G=	NP_001193863.1:n.*6G=