Canonical Allele Identifier: CA10538116
Community Standard Title: NM_005366.5(MAGEA11):c.247A>G (p.Ile83Val)
Gene: MAGEA11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149715658A>G , CM000685.2:g.149715658A>G GRCh38
NC_000023.10:g.148797318A>G , CM000685.1:g.148797318A>G GRCh37
NC_000023.9:g.148577087T>C NCBI36
NG_012803.1:g.32416A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005366.5:c.247A>G MANE Select NP_005357.2:p.Ile83Val
ENST00000355220.6:c.247A>G MANE Select ENSP00000347358.5:p.Ile83Val
NM_001011544.1:c.160A>G NP_001011544.1:p.Ile54Val
NM_001011544.2:c.160A>G NP_001011544.1:p.Ile54Val
NM_005366.4:c.247A>G NP_005357.2:p.Ile83Val
ENST00000333104.8:c.160A>G ENSP00000328177.4:p.Ile54Val
ENST00000355220.5:c.247A>G ENSP00000347358.5:p.Ile83Val
ENST00000412632.6:c.160A>G ENSP00000391496.2:p.Ile54Val
ENST00000518694.1:n.1837A>G
XM_011531163.1:c.247A>G XP_011529465.1:p.Ile83Val
XM_011531164.1:c.223A>G XP_011529466.1:p.Ile75Val
XM_011531164.2:c.223A>G XP_011529466.1:p.Ile75Val
XM_017029522.1:c.142A>G XP_016885011.1:p.Ile48Val