Canonical Allele Identifier: CA449827103
Gene: AGER HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32151453G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32183676G>C , CM000668.2:g.32183676G>C GRCh38
NC_000006.11:g.32151453G>C , CM000668.1:g.32151453G>C GRCh37
NC_000006.10:g.32259431G>C NCBI36
NG_029868.1:g.5647C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375076.9:c.234C>G MANE Select ENSP00000364217.4:p.Val78=
ENST00000375055.6:c.234C>G ENSP00000364195.2:p.Val78=
ENST00000375056.6:c.234C>G ENSP00000364196.2:p.Val78=
ENST00000375065.6:c.-182+282C>G ENSP00000364206.6:n.-182+282C>G
ENST00000375067.7:c.192C>G ENSP00000364208.3:p.Val64=
ENST00000375069.7:c.234C>G ENSP00000364210.4:p.Val78=
ENST00000375070.7:c.-70C>G ENSP00000364211.4:n.-70C>G
ENST00000375076.8:c.234C>G ENSP00000364217.4:p.Val78=
ENST00000438221.6:c.234C>G ENSP00000387887.2:p.Val78=
ENST00000450110.5:c.234C>G ENSP00000398466.1:p.Val78=
ENST00000484849.5:n.441C>G
ENST00000538695.2:c.234C>G ENSP00000445389.1:p.Val78=
ENST00000620802.4:c.234C>G ENSP00000484081.1:p.Val78=
NM_001136.4:c.234C>G NP_001127.1:p.Val78=
NM_001206929.1:c.234C>G NP_001193858.1:p.Val78=
NM_001206932.1:c.192C>G NP_001193861.1:p.Val64=
NM_001206934.1:c.234C>G NP_001193863.1:p.Val78=
NM_001206936.1:c.234C>G NP_001193865.1:p.Val78=
NM_001206940.1:c.234C>G NP_001193869.1:p.Val78=
NM_001206954.1:c.234C>G NP_001193883.1:p.Val78=
NM_001206966.1:c.234C>G NP_001193895.1:p.Val78=
NM_172197.2:c.192C>G NP_751947.1:p.Val64=
NR_038190.1:n.517C>G
XM_017010328.2:c.327C>G XP_016865817.1:p.Val109=
XR_001743189.2:n.392C>G
XR_001743190.2:n.392C>G
NM_001136.5:c.234C>G MANE Select NP_001127.1:p.Val78=
NM_001206932.2:c.192C>G NP_001193861.1:p.Val64=
NM_001206936.2:c.234C>G NP_001193865.1:p.Val78=
NM_001206940.2:c.234C>G NP_001193869.1:p.Val78=
NM_001206954.2:c.234C>G NP_001193883.1:p.Val78=
NM_001206966.2:c.234C>G NP_001193895.1:p.Val78=
NM_172197.3:c.192C>G NP_751947.1:p.Val64=
NR_038190.2:n.448C>G
NM_001206929.2:c.234C>G NP_001193858.1:p.Val78=
NM_001206934.2:c.234C>G NP_001193863.1:p.Val78=