Canonical Allele Identifier: CA363510006

Gene: AGER

Linked Data

• MyVariant Identifiers: chr6:g.32149178C>A (hg19) ; chr6:g.32181401C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32181401C>A , CM000668.2:g.32181401C>A	GRCh38
NC_000006.11:g.32149178C>A , CM000668.1:g.32149178C>A	GRCh37
NC_000006.10:g.32257156C>A	NCBI36
NG_029868.1:g.7922G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.1068G>T MANE Select	ENSP00000364217.4:p.Leu356=
ENST00000375055.6:c.*29+123G>T	ENSP00000364195.2:n.*29+123G>T
ENST00000375065.6:c.255G>T	ENSP00000364206.6:p.Leu85=
ENST00000375067.7:c.913G>T	ENSP00000364208.3:p.Ala305Ser
ENST00000375069.7:c.1116G>T	ENSP00000364210.4:p.Leu372=
ENST00000375070.7:c.738G>T	ENSP00000364211.4:p.Leu246=
ENST00000375076.8:c.1068G>T	ENSP00000364217.4:p.Leu356=
ENST00000438221.6:c.*29+123G>T	ENSP00000387887.2:n.*29+123G>T
ENST00000469940.5:n.235G>T
ENST00000473619.5:n.610G>T
ENST00000484849.5:n.1275G>T
ENST00000488669.5:n.615+123G>T
ENST00000620802.4:c.315G>T	ENSP00000484081.1:p.Leu105=
NM_001136.4:c.1068G>T	NP_001127.1:p.Leu356=
NM_001206929.1:c.1116G>T	NP_001193858.1:p.Leu372=
NM_001206932.1:c.1026G>T	NP_001193861.1:p.Leu342=
NM_001206934.1:c.*29+123G>T	NP_001193863.1:n.*29+123G>T
NM_001206936.1:c.1021+123G>T	NP_001193865.1:n.1021+123G>T
NM_001206940.1:c.*29+123G>T	NP_001193869.1:n.*29+123G>T
NM_001206954.1:c.931+123G>T	NP_001193883.1:n.931+123G>T
NM_001206966.1:c.*29+123G>T	NP_001193895.1:n.*29+123G>T
NM_172197.2:c.913G>T	NP_751947.1:p.Ala305Ser
NR_038190.1:n.1351G>T
XM_017010328.2:c.1072+123G>T	XP_016865817.1:n.1072+123G>T
XR_001743189.2:n.1132G>T
XR_001743190.2:n.1084G>T
NM_001136.5:c.1068G>T MANE Select	NP_001127.1:p.Leu356=
NM_001206932.2:c.1026G>T	NP_001193861.1:p.Leu342=
NM_001206936.2:c.1021+123G>T	NP_001193865.1:n.1021+123G>T
NM_001206940.2:c.*29+123G>T	NP_001193869.1:n.*29+123G>T
NM_001206954.2:c.931+123G>T	NP_001193883.1:n.931+123G>T
NM_001206966.2:c.*29+123G>T	NP_001193895.1:n.*29+123G>T
NM_172197.3:c.913G>T	NP_751947.1:p.Ala305Ser
NR_038190.2:n.1282G>T
NM_001206929.2:c.1116G>T	NP_001193858.1:p.Leu372=
NM_001206934.2:c.*29+123G>T	NP_001193863.1:n.*29+123G>T