Canonical Allele Identifier: CA1619452986

Gene: AGER

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32183574G= , CM000668.2:g.32183574G=	GRCh38
NC_000006.11:g.32151351G= , CM000668.1:g.32151351G=	GRCh37
NC_000006.10:g.32259329G=	NCBI36
NG_029868.1:g.5749C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375076.9:c.336C= MANE Select	ENSP00000364217.4:p.Asn112=
ENST00000375055.6:c.336C=	ENSP00000364195.2:p.Asn112=
ENST00000375056.6:c.336C=	ENSP00000364196.2:p.Asn112=
ENST00000375065.6:c.-182+384C=	ENSP00000364206.6:n.-182+384C=
ENST00000375067.7:c.294C=	ENSP00000364208.3:p.Asn98=
ENST00000375069.7:c.336C=	ENSP00000364210.4:p.Asn112=
ENST00000375070.7:c.33C=	ENSP00000364211.4:p.Asn11=
ENST00000375076.8:c.336C=	ENSP00000364217.4:p.Asn112=
ENST00000438221.6:c.336C=	ENSP00000387887.2:p.Asn112=
ENST00000450110.5:c.336C=	ENSP00000398466.1:p.Asn112=
ENST00000484849.5:n.543C=
ENST00000538695.2:c.336C=	ENSP00000445389.1:p.Asn112=
ENST00000620802.4:c.282+54C=	ENSP00000484081.1:n.282+54C=
NM_001136.4:c.336C=	NP_001127.1:p.Asn112=
NM_001206929.1:c.336C=	NP_001193858.1:p.Asn112=
NM_001206932.1:c.294C=	NP_001193861.1:p.Asn98=
NM_001206934.1:c.336C=	NP_001193863.1:p.Asn112=
NM_001206936.1:c.336C=	NP_001193865.1:p.Asn112=
NM_001206940.1:c.336C=	NP_001193869.1:p.Asn112=
NM_001206954.1:c.336C=	NP_001193883.1:p.Asn112=
NM_001206966.1:c.336C=	NP_001193895.1:p.Asn112=
NM_172197.2:c.294C=	NP_751947.1:p.Asn98=
NR_038190.1:n.619C=
XM_017010328.2:c.429C=	XP_016865817.1:p.Asn143=
XR_001743189.2:n.494C=
XR_001743190.2:n.494C=
NM_001136.5:c.336C= MANE Select	NP_001127.1:p.Asn112=
NM_001206932.2:c.294C=	NP_001193861.1:p.Asn98=
NM_001206936.2:c.336C=	NP_001193865.1:p.Asn112=
NM_001206940.2:c.336C=	NP_001193869.1:p.Asn112=
NM_001206954.2:c.336C=	NP_001193883.1:p.Asn112=
NM_001206966.2:c.336C=	NP_001193895.1:p.Asn112=
NM_172197.3:c.294C=	NP_751947.1:p.Asn98=
NR_038190.2:n.550C=
NM_001206929.2:c.336C=	NP_001193858.1:p.Asn112=
NM_001206934.2:c.336C=	NP_001193863.1:p.Asn112=