Canonical Allele Identifier: CA490090482

Gene: MYEF2 SLC24A5

Linked Data

• MyVariant Identifiers: chr15:g.48427086A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48134889A>T , CM000677.2:g.48134889A>T	GRCh38
NC_000015.9:g.48427086A>T , CM000677.1:g.48427086A>T	GRCh37
NC_000015.8:g.46214378A>T	NCBI36
NG_011500.1:g.18918A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324324.12:c.*8019T>A (MYEF2) MANE Select	ENSP00000316950.7:n.*8019T>A
ENST00000341459.8:c.495A>T (SLC24A5) MANE Select	ENSP00000341550.3:p.Ser165=
ENST00000324324.11:c.*8019T>A (MYEF2)	ENSP00000316950.7:n.*8019T>A
ENST00000341459.7:c.495A>T (SLC24A5)	ENSP00000341550.3:p.Ser165=
ENST00000449382.2:c.315A>T (SLC24A5)	ENSP00000389966.2:p.Ser105=
ENST00000463289.1:n.255A>T (SLC24A5)
NM_205850.2:c.495A>T (SLC24A5)	NP_995322.1:p.Ser165=
XM_011521458.1:c.516A>T (SLC24A5)	XP_011519760.1:p.Ser172=
XM_005254425.4:c.*8174T>A (MYEF2)	XP_005254482.2:n.*8174T>A
XM_017022079.1:c.249A>T (SLC24A5)	XP_016877568.1:p.Ser83=
XM_017022080.1:c.249A>T (SLC24A5)	XP_016877569.1:p.Ser83=
XM_017022285.1:c.*8174T>A (MYEF2)	XP_016877774.1:n.*8174T>A
XM_017022286.1:c.*8174T>A (MYEF2)	XP_016877775.1:n.*8174T>A
XM_017022287.1:c.*8174T>A (MYEF2)	XP_016877776.1:n.*8174T>A
XM_017022291.1:c.*8174T>A (MYEF2)	XP_016877780.1:n.*8174T>A
XM_017022292.1:c.*8174T>A (MYEF2)	XP_016877781.1:n.*8174T>A
XM_024449901.1:c.156A>T (SLC24A5)	XP_024305669.1:p.Ser52=
NM_016132.5:c.*8019T>A (MYEF2) MANE Select	NP_057216.3:n.*8019T>A
NM_001301210.2:c.*8019T>A (MYEF2)	NP_001288139.2:n.*8019T>A
NM_205850.3:c.495A>T (SLC24A5) MANE Select	NP_995322.1:p.Ser165=