Canonical Allele Identifier: CA2175374240

Gene: MYEF2 SLC24A5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48134922T= , CM000677.2:g.48134922T=	GRCh38
NC_000015.9:g.48427119T= , CM000677.1:g.48427119T=	GRCh37
NC_000015.8:g.46214411T=	NCBI36
NG_011500.1:g.18951T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324324.12:c.*7986A= (MYEF2) MANE Select	ENSP00000316950.7:n.*7986A=
ENST00000341459.8:c.528T= (SLC24A5) MANE Select	ENSP00000341550.3:p.Cys176=
ENST00000324324.11:c.*7986A= (MYEF2)	ENSP00000316950.7:n.*7986A=
ENST00000341459.7:c.528T= (SLC24A5)	ENSP00000341550.3:p.Cys176=
ENST00000449382.2:c.348T= (SLC24A5)	ENSP00000389966.2:p.Cys116=
ENST00000463289.1:n.288T= (SLC24A5)
NM_205850.2:c.528T= (SLC24A5)	NP_995322.1:p.Cys176=
XM_011521458.1:c.549T= (SLC24A5)	XP_011519760.1:p.Cys183=
XM_005254425.4:c.*8141A= (MYEF2)	XP_005254482.2:n.*8141A=
XM_017022079.1:c.282T= (SLC24A5)	XP_016877568.1:p.Cys94=
XM_017022080.1:c.282T= (SLC24A5)	XP_016877569.1:p.Cys94=
XM_017022285.1:c.*8141A= (MYEF2)	XP_016877774.1:n.*8141A=
XM_017022286.1:c.*8141A= (MYEF2)	XP_016877775.1:n.*8141A=
XM_017022287.1:c.*8141A= (MYEF2)	XP_016877776.1:n.*8141A=
XM_017022291.1:c.*8141A= (MYEF2)	XP_016877780.1:n.*8141A=
XM_017022292.1:c.*8141A= (MYEF2)	XP_016877781.1:n.*8141A=
XM_024449901.1:c.189T= (SLC24A5)	XP_024305669.1:p.Cys63=
NM_016132.5:c.*7986A= (MYEF2) MANE Select	NP_057216.3:n.*7986A=
NM_001301210.2:c.*7986A= (MYEF2)	NP_001288139.2:n.*7986A=
NM_205850.3:c.528T= (SLC24A5) MANE Select	NP_995322.1:p.Cys176=