Canonical Allele Identifier: CA2695115359

Gene: EMD

Linked Data

• gnomAD v4: X-154380815-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380815G>A , CM000685.2:g.154380815G>A	GRCh38
NC_000023.10:g.153609175G>A , CM000685.1:g.153609175G>A	GRCh37
NC_000023.9:g.153262369G>A	NCBI36
NG_008677.1:g.11380G>A , LRG_745:g.11380G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.449+13G>A	ENSP00000507245.1:n.449+13G>A
ENST00000682478.1:n.639+13G>A
ENST00000683576.1:n.639+13G>A
ENST00000683627.1:c.449+13G>A	ENSP00000507533.1:n.449+13G>A
ENST00000684082.1:c.406+13G>A	ENSP00000508266.1:n.406+13G>A
ENST00000684633.1:n.421+13G>A
ENST00000684678.1:c.445+13G>A	ENSP00000507059.1:n.445+13G>A
ENST00000369842.9:c.449+13G>A MANE Select	ENSP00000358857.4:n.449+13G>A
ENST00000369835.3:c.344+13G>A	ENSP00000358850.3:n.344+13G>A
ENST00000369842.8:c.449+13G>A	ENSP00000358857.4:n.449+13G>A
ENST00000428228.5:c.*354+13G>A	ENSP00000401081.1:n.*354+13G>A
ENST00000468294.5:n.422G>A
ENST00000471965.1:n.238+13G>A
ENST00000485261.1:n.652G>A
ENST00000486738.5:n.820G>A
ENST00000492448.1:n.432+13G>A
NM_000117.2:c.449+13G>A , LRG_745t1:c.449+13G>A	NP_000108.1:n.449+13G>A
XM_024452349.1:c.455+13G>A	XP_024308117.1:n.455+13G>A
NM_000117.3:c.449+13G>A MANE Select	NP_000108.1:n.449+13G>A