Canonical Allele Identifier: CA2466664360

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380892A= , CM000685.2:g.154380892A=	GRCh38
NC_000023.10:g.153609252A= , CM000685.1:g.153609252A=	GRCh37
NC_000023.9:g.153262446A=	NCBI36
NG_008677.1:g.11457A= , LRG_745:g.11457A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.460A=	ENSP00000507245.1:p.Met154=
ENST00000682478.1:n.650A=
ENST00000683576.1:n.650A=
ENST00000683627.1:c.460A=	ENSP00000507533.1:p.Met154=
ENST00000684082.1:c.417A=	ENSP00000508266.1:n.417A=
ENST00000684633.1:n.432A=
ENST00000684678.1:c.456A=	ENSP00000507059.1:n.456A=
ENST00000369842.9:c.460A= MANE Select	ENSP00000358857.4:p.Met154=
ENST00000369835.3:c.355A=	ENSP00000358850.3:p.Met119=
ENST00000369842.8:c.460A=	ENSP00000358857.4:p.Met154=
ENST00000428228.5:c.*365A=	ENSP00000401081.1:n.*365A=
ENST00000468294.5:n.499A=
ENST00000471965.1:n.249A=
ENST00000485261.1:n.729A=
ENST00000486738.5:n.897A=
ENST00000492448.1:n.443A=
NM_000117.2:c.460A= , LRG_745t1:c.460A=	NP_000108.1:p.Met154=
XM_024452349.1:c.466A=	XP_024308117.1:p.Met156=
NM_000117.3:c.460A= MANE Select	NP_000108.1:p.Met154=