Canonical Allele Identifier: CA392451045
Gene: MYEF2 HGNC NCBI
SLC24A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134950G>T , CM000677.2:g.48134950G>T GRCh38
NC_000015.9:g.48427147G>T , CM000677.1:g.48427147G>T GRCh37
NC_000015.8:g.46214439G>T NCBI36
NG_011500.1:g.18979G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000324324.12:c.*7958C>A (MYEF2) MANE Select ENSP00000316950.7:n.*7958C>A
ENST00000341459.8:c.556G>T (SLC24A5) MANE Select ENSP00000341550.3:p.Val186Phe
ENST00000324324.11:c.*7958C>A (MYEF2) ENSP00000316950.7:n.*7958C>A
ENST00000341459.7:c.556G>T (SLC24A5) ENSP00000341550.3:p.Val186Phe
ENST00000449382.2:c.376G>T (SLC24A5) ENSP00000389966.2:p.Val126Phe
ENST00000463289.1:n.316G>T (SLC24A5)
NM_205850.2:c.556G>T (SLC24A5) NP_995322.1:p.Val186Phe
XM_011521458.1:c.577G>T (SLC24A5) XP_011519760.1:p.Val193Phe
XM_005254425.4:c.*8113C>A (MYEF2) XP_005254482.2:n.*8113C>A
XM_017022079.1:c.310G>T (SLC24A5) XP_016877568.1:p.Val104Phe
XM_017022080.1:c.310G>T (SLC24A5) XP_016877569.1:p.Val104Phe
XM_017022285.1:c.*8113C>A (MYEF2) XP_016877774.1:n.*8113C>A
XM_017022286.1:c.*8113C>A (MYEF2) XP_016877775.1:n.*8113C>A
XM_017022287.1:c.*8113C>A (MYEF2) XP_016877776.1:n.*8113C>A
XM_017022291.1:c.*8113C>A (MYEF2) XP_016877780.1:n.*8113C>A
XM_017022292.1:c.*8113C>A (MYEF2) XP_016877781.1:n.*8113C>A
XM_024449901.1:c.217G>T (SLC24A5) XP_024305669.1:p.Val73Phe
NM_016132.5:c.*7958C>A (MYEF2) MANE Select NP_057216.3:n.*7958C>A
NM_001301210.2:c.*7958C>A (MYEF2) NP_001288139.2:n.*7958C>A
NM_205850.3:c.556G>T (SLC24A5) MANE Select NP_995322.1:p.Val186Phe