Canonical Allele Identifier: CA363509973

Gene: AGER

Linked Data

• MyVariant Identifiers: chr6:g.32149172A>G (hg19) ; chr6:g.32181395A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32181395A>G , CM000668.2:g.32181395A>G	GRCh38
NC_000006.11:g.32149172A>G , CM000668.1:g.32149172A>G	GRCh37
NC_000006.10:g.32257150A>G	NCBI36
NG_029868.1:g.7928T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.1074T>C MANE Select	ENSP00000364217.4:p.Ile358=
ENST00000375055.6:c.*29+129T>C	ENSP00000364195.2:n.*29+129T>C
ENST00000375065.6:c.261T>C	ENSP00000364206.6:p.Ile87=
ENST00000375067.7:c.919T>C	ENSP00000364208.3:p.Trp307Arg
ENST00000375069.7:c.1122T>C	ENSP00000364210.4:p.Ile374=
ENST00000375070.7:c.744T>C	ENSP00000364211.4:p.Ile248=
ENST00000375076.8:c.1074T>C	ENSP00000364217.4:p.Ile358=
ENST00000438221.6:c.*29+129T>C	ENSP00000387887.2:n.*29+129T>C
ENST00000469940.5:n.241T>C
ENST00000473619.5:n.616T>C
ENST00000484849.5:n.1281T>C
ENST00000488669.5:n.615+129T>C
ENST00000620802.4:c.321T>C	ENSP00000484081.1:p.Ile107=
NM_001136.4:c.1074T>C	NP_001127.1:p.Ile358=
NM_001206929.1:c.1122T>C	NP_001193858.1:p.Ile374=
NM_001206932.1:c.1032T>C	NP_001193861.1:p.Ile344=
NM_001206934.1:c.*29+129T>C	NP_001193863.1:n.*29+129T>C
NM_001206936.1:c.1021+129T>C	NP_001193865.1:n.1021+129T>C
NM_001206940.1:c.*29+129T>C	NP_001193869.1:n.*29+129T>C
NM_001206954.1:c.931+129T>C	NP_001193883.1:n.931+129T>C
NM_001206966.1:c.*29+129T>C	NP_001193895.1:n.*29+129T>C
NM_172197.2:c.919T>C	NP_751947.1:p.Trp307Arg
NR_038190.1:n.1357T>C
XM_017010328.2:c.1072+129T>C	XP_016865817.1:n.1072+129T>C
XR_001743189.2:n.1138T>C
XR_001743190.2:n.1090T>C
NM_001136.5:c.1074T>C MANE Select	NP_001127.1:p.Ile358=
NM_001206932.2:c.1032T>C	NP_001193861.1:p.Ile344=
NM_001206936.2:c.1021+129T>C	NP_001193865.1:n.1021+129T>C
NM_001206940.2:c.*29+129T>C	NP_001193869.1:n.*29+129T>C
NM_001206954.2:c.931+129T>C	NP_001193883.1:n.931+129T>C
NM_001206966.2:c.*29+129T>C	NP_001193895.1:n.*29+129T>C
NM_172197.3:c.919T>C	NP_751947.1:p.Trp307Arg
NR_038190.2:n.1288T>C
NM_001206929.2:c.1122T>C	NP_001193858.1:p.Ile374=
NM_001206934.2:c.*29+129T>C	NP_001193863.1:n.*29+129T>C