Canonical Allele Identifier: CA2695115008

Gene: EMD

Linked Data

• gnomAD v4: X-154379452-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379452G>A , CM000685.2:g.154379452G>A	GRCh38
NC_000023.10:g.153607812G>A , CM000685.1:g.153607812G>A	GRCh37
NC_000023.9:g.153261006G>A	NCBI36
NG_008677.1:g.10017G>A , LRG_745:g.10017G>A
NG_011506.1:g.195C>T
NG_011506.2:g.187C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.-33G>A	ENSP00000507245.1:n.-33G>A
ENST00000369842.9:c.-33G>A MANE Select	ENSP00000358857.4:n.-33G>A
ENST00000369835.3:c.-33G>A	ENSP00000358850.3:n.-33G>A
ENST00000369842.8:c.-33G>A	ENSP00000358857.4:n.-33G>A
ENST00000428228.5:c.-33G>A	ENSP00000401081.1:n.-33G>A
ENST00000485261.1:n.49G>A
ENST00000486738.5:n.112G>A
ENST00000494443.5:n.25G>A
NM_000117.2:c.-33G>A , LRG_745t1:c.-33G>A	NP_000108.1:n.-33G>A
XM_024452349.1:c.-241G>A	XP_024308117.1:n.-241G>A
NM_000117.3:c.-33G>A MANE Select	NP_000108.1:n.-33G>A