Canonical Allele Identifier: CA415258571

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609282A>T (hg19) ; chrX:g.154380922A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380922A>T , CM000685.2:g.154380922A>T	GRCh38
NC_000023.10:g.153609282A>T , CM000685.1:g.153609282A>T	GRCh37
NC_000023.9:g.153262476A>T	NCBI36
NG_008677.1:g.11487A>T , LRG_745:g.11487A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.490A>T	ENSP00000507245.1:p.Ile164Phe
ENST00000682478.1:n.680A>T
ENST00000683576.1:n.680A>T
ENST00000683627.1:c.490A>T	ENSP00000507533.1:p.Ile164Phe
ENST00000684082.1:c.447A>T	ENSP00000508266.1:n.447A>T
ENST00000684633.1:n.462A>T
ENST00000684678.1:c.486A>T	ENSP00000507059.1:n.486A>T
ENST00000369842.9:c.490A>T MANE Select	ENSP00000358857.4:p.Ile164Phe
ENST00000369835.3:c.385A>T	ENSP00000358850.3:p.Ile129Phe
ENST00000369842.8:c.490A>T	ENSP00000358857.4:p.Ile164Phe
ENST00000428228.5:c.*395A>T	ENSP00000401081.1:n.*395A>T
ENST00000471965.1:n.279A>T
ENST00000485261.1:n.759A>T
ENST00000486738.5:n.927A>T
ENST00000492448.1:n.473A>T
NM_000117.2:c.490A>T , LRG_745t1:c.490A>T	NP_000108.1:p.Ile164Phe
XM_024452349.1:c.496A>T	XP_024308117.1:p.Ile166Phe
NM_000117.3:c.490A>T MANE Select	NP_000108.1:p.Ile164Phe