Canonical Allele Identifier: CA392451026
Gene: MYEF2 HGNC NCBI
SLC24A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134941G>C , CM000677.2:g.48134941G>C GRCh38
NC_000015.9:g.48427138G>C , CM000677.1:g.48427138G>C GRCh37
NC_000015.8:g.46214430G>C NCBI36
NG_011500.1:g.18970G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324324.12:c.*7967C>G (MYEF2) MANE Select ENSP00000316950.7:n.*7967C>G
ENST00000341459.8:c.547G>C (SLC24A5) MANE Select ENSP00000341550.3:p.Ala183Pro
ENST00000324324.11:c.*7967C>G (MYEF2) ENSP00000316950.7:n.*7967C>G
ENST00000341459.7:c.547G>C (SLC24A5) ENSP00000341550.3:p.Ala183Pro
ENST00000449382.2:c.367G>C (SLC24A5) ENSP00000389966.2:p.Ala123Pro
ENST00000463289.1:n.307G>C (SLC24A5)
NM_205850.2:c.547G>C (SLC24A5) NP_995322.1:p.Ala183Pro
XM_011521458.1:c.568G>C (SLC24A5) XP_011519760.1:p.Ala190Pro
XM_005254425.4:c.*8122C>G (MYEF2) XP_005254482.2:n.*8122C>G
XM_017022079.1:c.301G>C (SLC24A5) XP_016877568.1:p.Ala101Pro
XM_017022080.1:c.301G>C (SLC24A5) XP_016877569.1:p.Ala101Pro
XM_017022285.1:c.*8122C>G (MYEF2) XP_016877774.1:n.*8122C>G
XM_017022286.1:c.*8122C>G (MYEF2) XP_016877775.1:n.*8122C>G
XM_017022287.1:c.*8122C>G (MYEF2) XP_016877776.1:n.*8122C>G
XM_017022291.1:c.*8122C>G (MYEF2) XP_016877780.1:n.*8122C>G
XM_017022292.1:c.*8122C>G (MYEF2) XP_016877781.1:n.*8122C>G
XM_024449901.1:c.208G>C (SLC24A5) XP_024305669.1:p.Ala70Pro
NM_016132.5:c.*7967C>G (MYEF2) MANE Select NP_057216.3:n.*7967C>G
NM_001301210.2:c.*7967C>G (MYEF2) NP_001288139.2:n.*7967C>G
NM_205850.3:c.547G>C (SLC24A5) MANE Select NP_995322.1:p.Ala183Pro