Canonical Allele Identifier: CA2839966759

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380725G>T , CM000685.2:g.154380725G>T	GRCh38
NC_000023.10:g.153609085G>T , CM000685.1:g.153609085G>T	GRCh37
NC_000023.9:g.153262279G>T	NCBI36
NG_008677.1:g.11290G>T , LRG_745:g.11290G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.400-28G>T	ENSP00000507245.1:n.400-28G>T
ENST00000682478.1:n.590-28G>T
ENST00000683576.1:n.590-28G>T
ENST00000683627.1:c.400-28G>T	ENSP00000507533.1:n.400-28G>T
ENST00000684082.1:c.357-28G>T	ENSP00000508266.1:n.357-28G>T
ENST00000684633.1:n.372-28G>T
ENST00000684678.1:c.396-28G>T	ENSP00000507059.1:n.396-28G>T
ENST00000369842.9:c.400-28G>T MANE Select	ENSP00000358857.4:n.400-28G>T
ENST00000369835.3:c.295-28G>T	ENSP00000358850.3:n.295-28G>T
ENST00000369842.8:c.400-28G>T	ENSP00000358857.4:n.400-28G>T
ENST00000428228.5:c.*305-28G>T	ENSP00000401081.1:n.*305-28G>T
ENST00000468294.5:n.360-28G>T
ENST00000471965.1:n.161G>T
ENST00000485261.1:n.590-28G>T
ENST00000486738.5:n.758-28G>T
ENST00000492448.1:n.383-28G>T
NM_000117.2:c.400-28G>T , LRG_745t1:c.400-28G>T	NP_000108.1:n.400-28G>T
XM_024452349.1:c.406-28G>T	XP_024308117.1:n.406-28G>T
NM_000117.3:c.400-28G>T MANE Select	NP_000108.1:n.400-28G>T