Canonical Allele Identifier: CA2579738444

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379444C>G , CM000685.2:g.154379444C>G	GRCh38
NC_000023.10:g.153607804C>G , CM000685.1:g.153607804C>G	GRCh37
NC_000023.9:g.153260998C>G	NCBI36
NG_008677.1:g.10009C>G , LRG_745:g.10009C>G
NG_011506.1:g.203G>C
NG_011506.2:g.195G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.-41C>G	ENSP00000507245.1:n.-41C>G
ENST00000369842.9:c.-41C>G MANE Select	ENSP00000358857.4:n.-41C>G
ENST00000369835.3:c.-41C>G	ENSP00000358850.3:n.-41C>G
ENST00000369842.8:c.-41C>G	ENSP00000358857.4:n.-41C>G
ENST00000428228.5:c.-41C>G	ENSP00000401081.1:n.-41C>G
ENST00000485261.1:n.41C>G
ENST00000486738.5:n.104C>G
ENST00000494443.5:n.17C>G
NM_000117.2:c.-41C>G , LRG_745t1:c.-41C>G	NP_000108.1:n.-41C>G
XM_024452349.1:c.-249C>G	XP_024308117.1:n.-249C>G
NM_000117.3:c.-41C>G MANE Select	NP_000108.1:n.-41C>G