Canonical Allele Identifier: CA3008793390

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380854_154380855insA , CM000685.2:g.154380854_154380855insA	GRCh38
NC_000023.10:g.153609214_153609215insA , CM000685.1:g.153609214_153609215insA	GRCh37
NC_000023.9:g.153262408_153262409insA	NCBI36
NG_008677.1:g.11419_11420insA , LRG_745:g.11419_11420insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.450-28_450-27insA	ENSP00000507245.1:n.450-28_450-27insA
ENST00000682478.1:n.640-28_640-27insA
ENST00000683576.1:n.640-28_640-27insA
ENST00000683627.1:c.450-28_450-27insA	ENSP00000507533.1:n.450-28_450-27insA
ENST00000684082.1:c.407-28_407-27insA	ENSP00000508266.1:n.407-28_407-27insA
ENST00000684633.1:n.422-28_422-27insA
ENST00000684678.1:c.446-28_446-27insA	ENSP00000507059.1:n.446-28_446-27insA
ENST00000369842.9:c.450-28_450-27insA MANE Select	ENSP00000358857.4:n.450-28_450-27insA
ENST00000369835.3:c.345-28_345-27insA	ENSP00000358850.3:n.345-28_345-27insA
ENST00000369842.8:c.450-28_450-27insA	ENSP00000358857.4:n.450-28_450-27insA
ENST00000428228.5:c.*355-28_*355-27insA	ENSP00000401081.1:n.*355-28_*355-27insA
ENST00000468294.5:n.461_462insA
ENST00000471965.1:n.239-28_239-27insA
ENST00000485261.1:n.691_692insA
ENST00000486738.5:n.859_860insA
ENST00000492448.1:n.433-28_433-27insA
NM_000117.2:c.450-28_450-27insA , LRG_745t1:c.450-28_450-27insA	NP_000108.1:n.450-28_450-27insA
XM_024452349.1:c.456-28_456-27insA	XP_024308117.1:n.456-28_456-27insA
NM_000117.3:c.450-28_450-27insA MANE Select	NP_000108.1:n.450-28_450-27insA