Canonical Allele Identifier: CA2526632581

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380153G>T , CM000685.2:g.154380153G>T	GRCh38
NC_000023.10:g.153608513G>T , CM000685.1:g.153608513G>T	GRCh37
NC_000023.9:g.153261707G>T	NCBI36
NG_008677.1:g.10718G>T , LRG_745:g.10718G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.266-81G>T	ENSP00000507245.1:n.266-81G>T
ENST00000682478.1:n.375G>T
ENST00000683576.1:n.375G>T
ENST00000683627.1:c.266-81G>T	ENSP00000507533.1:n.266-81G>T
ENST00000684082.1:c.266-124G>T	ENSP00000508266.1:n.266-124G>T
ENST00000684633.1:n.238-81G>T
ENST00000684678.1:c.262-81G>T	ENSP00000507059.1:n.262-81G>T
ENST00000369842.9:c.266-81G>T MANE Select	ENSP00000358857.4:n.266-81G>T
ENST00000369835.3:c.161-81G>T	ENSP00000358850.3:n.161-81G>T
ENST00000369842.8:c.266-81G>T	ENSP00000358857.4:n.266-81G>T
ENST00000428228.5:c.*171-81G>T	ENSP00000401081.1:n.*171-81G>T
ENST00000468294.5:n.226-81G>T
ENST00000485261.1:n.375G>T
ENST00000486738.5:n.543G>T
ENST00000492448.1:n.249-81G>T
ENST00000494443.5:n.456G>T
NM_000117.2:c.266-81G>T , LRG_745t1:c.266-81G>T	NP_000108.1:n.266-81G>T
XM_024452349.1:c.191G>T	XP_024308117.1:p.Arg64Leu
NM_000117.3:c.266-81G>T MANE Select	NP_000108.1:n.266-81G>T