Canonical Allele Identifier: CA392451032
Gene: MYEF2 HGNC NCBI
SLC24A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134944G>C , CM000677.2:g.48134944G>C GRCh38
NC_000015.9:g.48427141G>C , CM000677.1:g.48427141G>C GRCh37
NC_000015.8:g.46214433G>C NCBI36
NG_011500.1:g.18973G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000324324.12:c.*7964C>G (MYEF2) MANE Select ENSP00000316950.7:n.*7964C>G
ENST00000341459.8:c.550G>C (SLC24A5) MANE Select ENSP00000341550.3:p.Ala184Pro
ENST00000324324.11:c.*7964C>G (MYEF2) ENSP00000316950.7:n.*7964C>G
ENST00000341459.7:c.550G>C (SLC24A5) ENSP00000341550.3:p.Ala184Pro
ENST00000449382.2:c.370G>C (SLC24A5) ENSP00000389966.2:p.Ala124Pro
ENST00000463289.1:n.310G>C (SLC24A5)
NM_205850.2:c.550G>C (SLC24A5) NP_995322.1:p.Ala184Pro
XM_011521458.1:c.571G>C (SLC24A5) XP_011519760.1:p.Ala191Pro
XM_005254425.4:c.*8119C>G (MYEF2) XP_005254482.2:n.*8119C>G
XM_017022079.1:c.304G>C (SLC24A5) XP_016877568.1:p.Ala102Pro
XM_017022080.1:c.304G>C (SLC24A5) XP_016877569.1:p.Ala102Pro
XM_017022285.1:c.*8119C>G (MYEF2) XP_016877774.1:n.*8119C>G
XM_017022286.1:c.*8119C>G (MYEF2) XP_016877775.1:n.*8119C>G
XM_017022287.1:c.*8119C>G (MYEF2) XP_016877776.1:n.*8119C>G
XM_017022291.1:c.*8119C>G (MYEF2) XP_016877780.1:n.*8119C>G
XM_017022292.1:c.*8119C>G (MYEF2) XP_016877781.1:n.*8119C>G
XM_024449901.1:c.211G>C (SLC24A5) XP_024305669.1:p.Ala71Pro
NM_016132.5:c.*7964C>G (MYEF2) MANE Select NP_057216.3:n.*7964C>G
NM_001301210.2:c.*7964C>G (MYEF2) NP_001288139.2:n.*7964C>G
NM_205850.3:c.550G>C (SLC24A5) MANE Select NP_995322.1:p.Ala184Pro