Canonical Allele Identifier: CA1619453025

Gene: AGER

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32183617C= , CM000668.2:g.32183617C=	GRCh38
NC_000006.11:g.32151394C= , CM000668.1:g.32151394C=	GRCh37
NC_000006.10:g.32259372C=	NCBI36
NG_029868.1:g.5706G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.293G= MANE Select	ENSP00000364217.4:p.Arg98=
ENST00000375055.6:c.293G=	ENSP00000364195.2:p.Arg98=
ENST00000375056.6:c.293G=	ENSP00000364196.2:p.Arg98=
ENST00000375065.6:c.-182+341G=	ENSP00000364206.6:n.-182+341G=
ENST00000375067.7:c.251G=	ENSP00000364208.3:p.Arg84=
ENST00000375069.7:c.293G=	ENSP00000364210.4:p.Arg98=
ENST00000375070.7:c.-11G=	ENSP00000364211.4:n.-11G=
ENST00000375076.8:c.293G=	ENSP00000364217.4:p.Arg98=
ENST00000438221.6:c.293G=	ENSP00000387887.2:p.Arg98=
ENST00000450110.5:c.293G=	ENSP00000398466.1:p.Arg98=
ENST00000484849.5:n.500G=
ENST00000538695.2:c.293G=	ENSP00000445389.1:p.Arg98=
ENST00000620802.4:c.282+11G=	ENSP00000484081.1:n.282+11G=
NM_001136.4:c.293G=	NP_001127.1:p.Arg98=
NM_001206929.1:c.293G=	NP_001193858.1:p.Arg98=
NM_001206932.1:c.251G=	NP_001193861.1:p.Arg84=
NM_001206934.1:c.293G=	NP_001193863.1:p.Arg98=
NM_001206936.1:c.293G=	NP_001193865.1:p.Arg98=
NM_001206940.1:c.293G=	NP_001193869.1:p.Arg98=
NM_001206954.1:c.293G=	NP_001193883.1:p.Arg98=
NM_001206966.1:c.293G=	NP_001193895.1:p.Arg98=
NM_172197.2:c.251G=	NP_751947.1:p.Arg84=
NR_038190.1:n.576G=
XM_017010328.2:c.386G=	XP_016865817.1:p.Arg129=
XR_001743189.2:n.451G=
XR_001743190.2:n.451G=
NM_001136.5:c.293G= MANE Select	NP_001127.1:p.Arg98=
NM_001206932.2:c.251G=	NP_001193861.1:p.Arg84=
NM_001206936.2:c.293G=	NP_001193865.1:p.Arg98=
NM_001206940.2:c.293G=	NP_001193869.1:p.Arg98=
NM_001206954.2:c.293G=	NP_001193883.1:p.Arg98=
NM_001206966.2:c.293G=	NP_001193895.1:p.Arg98=
NM_172197.3:c.251G=	NP_751947.1:p.Arg84=
NR_038190.2:n.507G=
NM_001206929.2:c.293G=	NP_001193858.1:p.Arg98=
NM_001206934.2:c.293G=	NP_001193863.1:p.Arg98=