Canonical Allele Identifier: CA363509745

Gene: AGER

Linked Data

• MyVariant Identifiers: chr6:g.32149129T>G (hg19) ; chr6:g.32181352T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32181352T>G , CM000668.2:g.32181352T>G	GRCh38
NC_000006.11:g.32149129T>G , CM000668.1:g.32149129T>G	GRCh37
NC_000006.10:g.32257107T>G	NCBI36
NG_029868.1:g.7971A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.1117A>C MANE Select	ENSP00000364217.4:p.Arg373=
ENST00000375055.6:c.*30-113A>C	ENSP00000364195.2:n.*30-113A>C
ENST00000375065.6:c.304A>C	ENSP00000364206.6:p.Arg102=
ENST00000375067.7:c.962A>C	ENSP00000364208.3:p.Glu321Ala
ENST00000375069.7:c.1165A>C	ENSP00000364210.4:p.Arg389=
ENST00000375070.7:c.787A>C	ENSP00000364211.4:p.Arg263=
ENST00000375076.8:c.1117A>C	ENSP00000364217.4:p.Arg373=
ENST00000438221.6:c.*30-113A>C	ENSP00000387887.2:n.*30-113A>C
ENST00000469940.5:n.284A>C
ENST00000473619.5:n.659A>C
ENST00000484849.5:n.1324A>C
ENST00000488669.5:n.616-113A>C
ENST00000620802.4:c.364A>C	ENSP00000484081.1:p.Arg122=
NM_001136.4:c.1117A>C	NP_001127.1:p.Arg373=
NM_001206929.1:c.1165A>C	NP_001193858.1:p.Arg389=
NM_001206932.1:c.1075A>C	NP_001193861.1:p.Arg359=
NM_001206934.1:c.*30-113A>C	NP_001193863.1:n.*30-113A>C
NM_001206936.1:c.1022-113A>C	NP_001193865.1:n.1022-113A>C
NM_001206940.1:c.*30-113A>C	NP_001193869.1:n.*30-113A>C
NM_001206954.1:c.932-113A>C	NP_001193883.1:n.932-113A>C
NM_001206966.1:c.*29+172A>C	NP_001193895.1:n.*29+172A>C
NM_172197.2:c.962A>C	NP_751947.1:p.Glu321Ala
NR_038190.1:n.1400A>C
XM_017010328.2:c.1073-113A>C	XP_016865817.1:n.1073-113A>C
XR_001743189.2:n.1181A>C
XR_001743190.2:n.1133A>C
NM_001136.5:c.1117A>C MANE Select	NP_001127.1:p.Arg373=
NM_001206932.2:c.1075A>C	NP_001193861.1:p.Arg359=
NM_001206936.2:c.1022-113A>C	NP_001193865.1:n.1022-113A>C
NM_001206940.2:c.*30-113A>C	NP_001193869.1:n.*30-113A>C
NM_001206954.2:c.932-113A>C	NP_001193883.1:n.932-113A>C
NM_001206966.2:c.*29+172A>C	NP_001193895.1:n.*29+172A>C
NM_172197.3:c.962A>C	NP_751947.1:p.Glu321Ala
NR_038190.2:n.1331A>C
NM_001206929.2:c.1165A>C	NP_001193858.1:p.Arg389=
NM_001206934.2:c.*30-113A>C	NP_001193863.1:n.*30-113A>C