Canonical Allele Identifier: CA363510067

Gene: AGER

Linked Data

• MyVariant Identifiers: chr6:g.32149188G>T (hg19) ; chr6:g.32181411G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32181411G>T , CM000668.2:g.32181411G>T	GRCh38
NC_000006.11:g.32149188G>T , CM000668.1:g.32149188G>T	GRCh37
NC_000006.10:g.32257166G>T	NCBI36
NG_029868.1:g.7912C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.1058C>A MANE Select	ENSP00000364217.4:p.Thr353Lys
ENST00000375055.6:c.*29+113C>A	ENSP00000364195.2:n.*29+113C>A
ENST00000375065.6:c.245C>A	ENSP00000364206.6:p.Thr82Lys
ENST00000375067.7:c.903C>A	ENSP00000364208.3:p.Asp301Glu
ENST00000375069.7:c.1106C>A	ENSP00000364210.4:p.Thr369Lys
ENST00000375070.7:c.728C>A	ENSP00000364211.4:p.Thr243Lys
ENST00000375076.8:c.1058C>A	ENSP00000364217.4:p.Thr353Lys
ENST00000438221.6:c.*29+113C>A	ENSP00000387887.2:n.*29+113C>A
ENST00000469940.5:n.225C>A
ENST00000473619.5:n.600C>A
ENST00000484849.5:n.1265C>A
ENST00000488669.5:n.615+113C>A
ENST00000620802.4:c.305C>A	ENSP00000484081.1:p.Thr102Lys
NM_001136.4:c.1058C>A	NP_001127.1:p.Thr353Lys
NM_001206929.1:c.1106C>A	NP_001193858.1:p.Thr369Lys
NM_001206932.1:c.1016C>A	NP_001193861.1:p.Thr339Lys
NM_001206934.1:c.*29+113C>A	NP_001193863.1:n.*29+113C>A
NM_001206936.1:c.1021+113C>A	NP_001193865.1:n.1021+113C>A
NM_001206940.1:c.*29+113C>A	NP_001193869.1:n.*29+113C>A
NM_001206954.1:c.931+113C>A	NP_001193883.1:n.931+113C>A
NM_001206966.1:c.*29+113C>A	NP_001193895.1:n.*29+113C>A
NM_172197.2:c.903C>A	NP_751947.1:p.Asp301Glu
NR_038190.1:n.1341C>A
XM_017010328.2:c.1072+113C>A	XP_016865817.1:n.1072+113C>A
XR_001743189.2:n.1122C>A
XR_001743190.2:n.1074C>A
NM_001136.5:c.1058C>A MANE Select	NP_001127.1:p.Thr353Lys
NM_001206932.2:c.1016C>A	NP_001193861.1:p.Thr339Lys
NM_001206936.2:c.1021+113C>A	NP_001193865.1:n.1021+113C>A
NM_001206940.2:c.*29+113C>A	NP_001193869.1:n.*29+113C>A
NM_001206954.2:c.931+113C>A	NP_001193883.1:n.931+113C>A
NM_001206966.2:c.*29+113C>A	NP_001193895.1:n.*29+113C>A
NM_172197.3:c.903C>A	NP_751947.1:p.Asp301Glu
NR_038190.2:n.1272C>A
NM_001206929.2:c.1106C>A	NP_001193858.1:p.Thr369Lys
NM_001206934.2:c.*29+113C>A	NP_001193863.1:n.*29+113C>A