Canonical Allele Identifier: CA363509823

Gene: AGER

Linked Data

• MyVariant Identifiers: chr6:g.32149145T>A (hg19) ; chr6:g.32181368T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32181368T>A , CM000668.2:g.32181368T>A	GRCh38
NC_000006.11:g.32149145T>A , CM000668.1:g.32149145T>A	GRCh37
NC_000006.10:g.32257123T>A	NCBI36
NG_029868.1:g.7955A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.1101A>T MANE Select	ENSP00000364217.4:p.Gln367His
ENST00000375055.6:c.*30-129A>T	ENSP00000364195.2:n.*30-129A>T
ENST00000375065.6:c.288A>T	ENSP00000364206.6:p.Gln96His
ENST00000375067.7:c.946A>T	ENSP00000364208.3:p.Thr316Ser
ENST00000375069.7:c.1149A>T	ENSP00000364210.4:p.Gln383His
ENST00000375070.7:c.771A>T	ENSP00000364211.4:p.Gln257His
ENST00000375076.8:c.1101A>T	ENSP00000364217.4:p.Gln367His
ENST00000438221.6:c.*30-129A>T	ENSP00000387887.2:n.*30-129A>T
ENST00000469940.5:n.268A>T
ENST00000473619.5:n.643A>T
ENST00000484849.5:n.1308A>T
ENST00000488669.5:n.616-129A>T
ENST00000620802.4:c.348A>T	ENSP00000484081.1:p.Gln116His
NM_001136.4:c.1101A>T	NP_001127.1:p.Gln367His
NM_001206929.1:c.1149A>T	NP_001193858.1:p.Gln383His
NM_001206932.1:c.1059A>T	NP_001193861.1:p.Gln353His
NM_001206934.1:c.*30-129A>T	NP_001193863.1:n.*30-129A>T
NM_001206936.1:c.1022-129A>T	NP_001193865.1:n.1022-129A>T
NM_001206940.1:c.*30-129A>T	NP_001193869.1:n.*30-129A>T
NM_001206954.1:c.932-129A>T	NP_001193883.1:n.932-129A>T
NM_001206966.1:c.*29+156A>T	NP_001193895.1:n.*29+156A>T
NM_172197.2:c.946A>T	NP_751947.1:p.Thr316Ser
NR_038190.1:n.1384A>T
XM_017010328.2:c.1073-129A>T	XP_016865817.1:n.1073-129A>T
XR_001743189.2:n.1165A>T
XR_001743190.2:n.1117A>T
NM_001136.5:c.1101A>T MANE Select	NP_001127.1:p.Gln367His
NM_001206932.2:c.1059A>T	NP_001193861.1:p.Gln353His
NM_001206936.2:c.1022-129A>T	NP_001193865.1:n.1022-129A>T
NM_001206940.2:c.*30-129A>T	NP_001193869.1:n.*30-129A>T
NM_001206954.2:c.932-129A>T	NP_001193883.1:n.932-129A>T
NM_001206966.2:c.*29+156A>T	NP_001193895.1:n.*29+156A>T
NM_172197.3:c.946A>T	NP_751947.1:p.Thr316Ser
NR_038190.2:n.1315A>T
NM_001206929.2:c.1149A>T	NP_001193858.1:p.Gln383His
NM_001206934.2:c.*30-129A>T	NP_001193863.1:n.*30-129A>T