Canonical Allele Identifier: CA392450469

Gene: MYEF2 SLC24A5

Linked Data

• MyVariant Identifiers: chr15:g.48427103C>A (hg19) ; chr15:g.48134906C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48134906C>A , CM000677.2:g.48134906C>A	GRCh38
NC_000015.9:g.48427103C>A , CM000677.1:g.48427103C>A	GRCh37
NC_000015.8:g.46214395C>A	NCBI36
NG_011500.1:g.18935C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324324.12:c.*8002G>T (MYEF2) MANE Select	ENSP00000316950.7:n.*8002G>T
ENST00000341459.8:c.512C>A (SLC24A5) MANE Select	ENSP00000341550.3:p.Pro171His
ENST00000324324.11:c.*8002G>T (MYEF2)	ENSP00000316950.7:n.*8002G>T
ENST00000341459.7:c.512C>A (SLC24A5)	ENSP00000341550.3:p.Pro171His
ENST00000449382.2:c.332C>A (SLC24A5)	ENSP00000389966.2:p.Pro111His
ENST00000463289.1:n.272C>A (SLC24A5)
NM_205850.2:c.512C>A (SLC24A5)	NP_995322.1:p.Pro171His
XM_011521458.1:c.533C>A (SLC24A5)	XP_011519760.1:p.Pro178His
XM_005254425.4:c.*8157G>T (MYEF2)	XP_005254482.2:n.*8157G>T
XM_017022079.1:c.266C>A (SLC24A5)	XP_016877568.1:p.Pro89His
XM_017022080.1:c.266C>A (SLC24A5)	XP_016877569.1:p.Pro89His
XM_017022285.1:c.*8157G>T (MYEF2)	XP_016877774.1:n.*8157G>T
XM_017022286.1:c.*8157G>T (MYEF2)	XP_016877775.1:n.*8157G>T
XM_017022287.1:c.*8157G>T (MYEF2)	XP_016877776.1:n.*8157G>T
XM_017022291.1:c.*8157G>T (MYEF2)	XP_016877780.1:n.*8157G>T
XM_017022292.1:c.*8157G>T (MYEF2)	XP_016877781.1:n.*8157G>T
XM_024449901.1:c.173C>A (SLC24A5)	XP_024305669.1:p.Pro58His
NM_016132.5:c.*8002G>T (MYEF2) MANE Select	NP_057216.3:n.*8002G>T
NM_001301210.2:c.*8002G>T (MYEF2)	NP_001288139.2:n.*8002G>T
NM_205850.3:c.512C>A (SLC24A5) MANE Select	NP_995322.1:p.Pro171His