Canonical Allele Identifier: CA363510042

Gene: AGER

Linked Data

• MyVariant Identifiers: chr6:g.32149184G>C (hg19) ; chr6:g.32181407G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32181407G>C , CM000668.2:g.32181407G>C	GRCh38
NC_000006.11:g.32149184G>C , CM000668.1:g.32149184G>C	GRCh37
NC_000006.10:g.32257162G>C	NCBI36
NG_029868.1:g.7916C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000375076.9:c.1062C>G MANE Select	ENSP00000364217.4:p.Ala354=
ENST00000375055.6:c.*29+117C>G	ENSP00000364195.2:n.*29+117C>G
ENST00000375065.6:c.249C>G	ENSP00000364206.6:p.Ala83=
ENST00000375067.7:c.907C>G	ENSP00000364208.3:p.Arg303Gly
ENST00000375069.7:c.1110C>G	ENSP00000364210.4:p.Ala370=
ENST00000375070.7:c.732C>G	ENSP00000364211.4:p.Ala244=
ENST00000375076.8:c.1062C>G	ENSP00000364217.4:p.Ala354=
ENST00000438221.6:c.*29+117C>G	ENSP00000387887.2:n.*29+117C>G
ENST00000469940.5:n.229C>G
ENST00000473619.5:n.604C>G
ENST00000484849.5:n.1269C>G
ENST00000488669.5:n.615+117C>G
ENST00000620802.4:c.309C>G	ENSP00000484081.1:p.Ala103=
NM_001136.4:c.1062C>G	NP_001127.1:p.Ala354=
NM_001206929.1:c.1110C>G	NP_001193858.1:p.Ala370=
NM_001206932.1:c.1020C>G	NP_001193861.1:p.Ala340=
NM_001206934.1:c.*29+117C>G	NP_001193863.1:n.*29+117C>G
NM_001206936.1:c.1021+117C>G	NP_001193865.1:n.1021+117C>G
NM_001206940.1:c.*29+117C>G	NP_001193869.1:n.*29+117C>G
NM_001206954.1:c.931+117C>G	NP_001193883.1:n.931+117C>G
NM_001206966.1:c.*29+117C>G	NP_001193895.1:n.*29+117C>G
NM_172197.2:c.907C>G	NP_751947.1:p.Arg303Gly
NR_038190.1:n.1345C>G
XM_017010328.2:c.1072+117C>G	XP_016865817.1:n.1072+117C>G
XR_001743189.2:n.1126C>G
XR_001743190.2:n.1078C>G
NM_001136.5:c.1062C>G MANE Select	NP_001127.1:p.Ala354=
NM_001206932.2:c.1020C>G	NP_001193861.1:p.Ala340=
NM_001206936.2:c.1021+117C>G	NP_001193865.1:n.1021+117C>G
NM_001206940.2:c.*29+117C>G	NP_001193869.1:n.*29+117C>G
NM_001206954.2:c.931+117C>G	NP_001193883.1:n.931+117C>G
NM_001206966.2:c.*29+117C>G	NP_001193895.1:n.*29+117C>G
NM_172197.3:c.907C>G	NP_751947.1:p.Arg303Gly
NR_038190.2:n.1276C>G
NM_001206929.2:c.1110C>G	NP_001193858.1:p.Ala370=
NM_001206934.2:c.*29+117C>G	NP_001193863.1:n.*29+117C>G