Canonical Allele Identifier: CA2579738443

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379442G>T , CM000685.2:g.154379442G>T	GRCh38
NC_000023.10:g.153607802G>T , CM000685.1:g.153607802G>T	GRCh37
NC_000023.9:g.153260996G>T	NCBI36
NG_008677.1:g.10007G>T , LRG_745:g.10007G>T
NG_011506.1:g.205C>A
NG_011506.2:g.197C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.-43G>T	ENSP00000507245.1:n.-43G>T
ENST00000369842.9:c.-43G>T MANE Select	ENSP00000358857.4:n.-43G>T
ENST00000369835.3:c.-43G>T	ENSP00000358850.3:n.-43G>T
ENST00000369842.8:c.-43G>T	ENSP00000358857.4:n.-43G>T
ENST00000428228.5:c.-43G>T	ENSP00000401081.1:n.-43G>T
ENST00000485261.1:n.39G>T
ENST00000486738.5:n.102G>T
ENST00000494443.5:n.15G>T
NM_000117.2:c.-43G>T , LRG_745t1:c.-43G>T	NP_000108.1:n.-43G>T
XM_024452349.1:c.-251G>T	XP_024308117.1:n.-251G>T
NM_000117.3:c.-43G>T MANE Select	NP_000108.1:n.-43G>T