Canonical Allele Identifier: CA363518934

Gene: AGER

Linked Data

• dbSNP Id: rs2127440408
• MyVariant Identifiers: chr6:g.32151353T>C (hg19) ; chr6:g.32183576T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32183576T>C , CM000668.2:g.32183576T>C	GRCh38
NC_000006.11:g.32151353T>C , CM000668.1:g.32151353T>C	GRCh37
NC_000006.10:g.32259331T>C	NCBI36
NG_029868.1:g.5747A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000375076.9:c.334A>G MANE Select	ENSP00000364217.4:p.Asn112Asp
ENST00000375055.6:c.334A>G	ENSP00000364195.2:p.Asn112Asp
ENST00000375056.6:c.334A>G	ENSP00000364196.2:p.Asn112Asp
ENST00000375065.6:c.-182+382A>G	ENSP00000364206.6:n.-182+382A>G
ENST00000375067.7:c.292A>G	ENSP00000364208.3:p.Asn98Asp
ENST00000375069.7:c.334A>G	ENSP00000364210.4:p.Asn112Asp
ENST00000375070.7:c.31A>G	ENSP00000364211.4:p.Asn11Asp
ENST00000375076.8:c.334A>G	ENSP00000364217.4:p.Asn112Asp
ENST00000438221.6:c.334A>G	ENSP00000387887.2:p.Asn112Asp
ENST00000450110.5:c.334A>G	ENSP00000398466.1:p.Asn112Asp
ENST00000484849.5:n.541A>G
ENST00000538695.2:c.334A>G	ENSP00000445389.1:p.Asn112Asp
ENST00000620802.4:c.282+52A>G	ENSP00000484081.1:n.282+52A>G
NM_001136.4:c.334A>G	NP_001127.1:p.Asn112Asp
NM_001206929.1:c.334A>G	NP_001193858.1:p.Asn112Asp
NM_001206932.1:c.292A>G	NP_001193861.1:p.Asn98Asp
NM_001206934.1:c.334A>G	NP_001193863.1:p.Asn112Asp
NM_001206936.1:c.334A>G	NP_001193865.1:p.Asn112Asp
NM_001206940.1:c.334A>G	NP_001193869.1:p.Asn112Asp
NM_001206954.1:c.334A>G	NP_001193883.1:p.Asn112Asp
NM_001206966.1:c.334A>G	NP_001193895.1:p.Asn112Asp
NM_172197.2:c.292A>G	NP_751947.1:p.Asn98Asp
NR_038190.1:n.617A>G
XM_017010328.2:c.427A>G	XP_016865817.1:p.Asn143Asp
XR_001743189.2:n.492A>G
XR_001743190.2:n.492A>G
NM_001136.5:c.334A>G MANE Select	NP_001127.1:p.Asn112Asp
NM_001206932.2:c.292A>G	NP_001193861.1:p.Asn98Asp
NM_001206936.2:c.334A>G	NP_001193865.1:p.Asn112Asp
NM_001206940.2:c.334A>G	NP_001193869.1:p.Asn112Asp
NM_001206954.2:c.334A>G	NP_001193883.1:p.Asn112Asp
NM_001206966.2:c.334A>G	NP_001193895.1:p.Asn112Asp
NM_172197.3:c.292A>G	NP_751947.1:p.Asn98Asp
NR_038190.2:n.548A>G
NM_001206929.2:c.334A>G	NP_001193858.1:p.Asn112Asp
NM_001206934.2:c.334A>G	NP_001193863.1:p.Asn112Asp