Canonical Allele Identifier: CA363510890

Gene: AGER

Linked Data

• MyVariant Identifiers: chr6:g.32149387A>T (hg19) ; chr6:g.32181610A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32181610A>T , CM000668.2:g.32181610A>T	GRCh38
NC_000006.11:g.32149387A>T , CM000668.1:g.32149387A>T	GRCh37
NC_000006.10:g.32257365A>T	NCBI36
NG_029868.1:g.7713T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.987T>A MANE Select	ENSP00000364217.4:p.Thr329=
ENST00000375055.6:c.987T>A	ENSP00000364195.2:p.Thr329=
ENST00000375065.6:c.174T>A	ENSP00000364206.6:p.Thr58=
ENST00000375067.7:c.832T>A	ENSP00000364208.3:p.Cys278Ser
ENST00000375069.7:c.1035T>A	ENSP00000364210.4:p.Thr345=
ENST00000375070.7:c.662-133T>A	ENSP00000364211.4:n.662-133T>A
ENST00000375076.8:c.987T>A	ENSP00000364217.4:p.Thr329=
ENST00000438221.6:c.1035T>A	ENSP00000387887.2:p.Thr345=
ENST00000469940.5:n.26T>A
ENST00000473619.5:n.529T>A
ENST00000484849.5:n.1194T>A
ENST00000488669.5:n.529T>A
ENST00000620802.4:c.283-177T>A	ENSP00000484081.1:n.283-177T>A
NM_001136.4:c.987T>A	NP_001127.1:p.Thr329=
NM_001206929.1:c.1035T>A	NP_001193858.1:p.Thr345=
NM_001206932.1:c.945T>A	NP_001193861.1:p.Thr315=
NM_001206934.1:c.1035T>A	NP_001193863.1:p.Thr345=
NM_001206936.1:c.935T>A	NP_001193865.1:p.Leu312Gln
NM_001206940.1:c.987T>A	NP_001193869.1:p.Thr329=
NM_001206954.1:c.845T>A	NP_001193883.1:p.Leu282Gln
NM_001206966.1:c.987T>A	NP_001193895.1:p.Thr329=
NM_172197.2:c.832T>A	NP_751947.1:p.Cys278Ser
NR_038190.1:n.1270T>A
XM_017010328.2:c.986T>A	XP_016865817.1:p.Leu329Gln
XR_001743189.2:n.1051T>A
XR_001743190.2:n.1003T>A
NM_001136.5:c.987T>A MANE Select	NP_001127.1:p.Thr329=
NM_001206932.2:c.945T>A	NP_001193861.1:p.Thr315=
NM_001206936.2:c.935T>A	NP_001193865.1:p.Leu312Gln
NM_001206940.2:c.987T>A	NP_001193869.1:p.Thr329=
NM_001206954.2:c.845T>A	NP_001193883.1:p.Leu282Gln
NM_001206966.2:c.987T>A	NP_001193895.1:p.Thr329=
NM_172197.3:c.832T>A	NP_751947.1:p.Cys278Ser
NR_038190.2:n.1201T>A
NM_001206929.2:c.1035T>A	NP_001193858.1:p.Thr345=
NM_001206934.2:c.1035T>A	NP_001193863.1:p.Thr345=