Canonical Allele Identifier: CA392450453
Gene: MYEF2 HGNC NCBI
SLC24A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134900G>C , CM000677.2:g.48134900G>C GRCh38
NC_000015.9:g.48427097G>C , CM000677.1:g.48427097G>C GRCh37
NC_000015.8:g.46214389G>C NCBI36
NG_011500.1:g.18929G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324324.12:c.*8008C>G (MYEF2) MANE Select ENSP00000316950.7:n.*8008C>G
ENST00000341459.8:c.506G>C (SLC24A5) MANE Select ENSP00000341550.3:p.Cys169Ser
ENST00000324324.11:c.*8008C>G (MYEF2) ENSP00000316950.7:n.*8008C>G
ENST00000341459.7:c.506G>C (SLC24A5) ENSP00000341550.3:p.Cys169Ser
ENST00000449382.2:c.326G>C (SLC24A5) ENSP00000389966.2:p.Cys109Ser
ENST00000463289.1:n.266G>C (SLC24A5)
NM_205850.2:c.506G>C (SLC24A5) NP_995322.1:p.Cys169Ser
XM_011521458.1:c.527G>C (SLC24A5) XP_011519760.1:p.Cys176Ser
XM_005254425.4:c.*8163C>G (MYEF2) XP_005254482.2:n.*8163C>G
XM_017022079.1:c.260G>C (SLC24A5) XP_016877568.1:p.Cys87Ser
XM_017022080.1:c.260G>C (SLC24A5) XP_016877569.1:p.Cys87Ser
XM_017022285.1:c.*8163C>G (MYEF2) XP_016877774.1:n.*8163C>G
XM_017022286.1:c.*8163C>G (MYEF2) XP_016877775.1:n.*8163C>G
XM_017022287.1:c.*8163C>G (MYEF2) XP_016877776.1:n.*8163C>G
XM_017022291.1:c.*8163C>G (MYEF2) XP_016877780.1:n.*8163C>G
XM_017022292.1:c.*8163C>G (MYEF2) XP_016877781.1:n.*8163C>G
XM_024449901.1:c.167G>C (SLC24A5) XP_024305669.1:p.Cys56Ser
NM_016132.5:c.*8008C>G (MYEF2) MANE Select NP_057216.3:n.*8008C>G
NM_001301210.2:c.*8008C>G (MYEF2) NP_001288139.2:n.*8008C>G
NM_205850.3:c.506G>C (SLC24A5) MANE Select NP_995322.1:p.Cys169Ser