Canonical Allele Identifier: CA2509396190

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379676_154379677insA , CM000685.2:g.154379676_154379677insA	GRCh38
NC_000023.10:g.153608036_153608037insA , CM000685.1:g.153608036_153608037insA	GRCh37
NC_000023.9:g.153261230_153261231insA	NCBI36
NG_008677.1:g.10241_10242insA , LRG_745:g.10241_10242insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.83-14_83-13insA	ENSP00000507245.1:n.83-14_83-13insA
ENST00000682478.1:n.59-14_59-13insA
ENST00000683576.1:n.59-14_59-13insA
ENST00000683627.1:c.83-14_83-13insA	ENSP00000507533.1:n.83-14_83-13insA
ENST00000684082.1:c.83-14_83-13insA	ENSP00000508266.1:n.83-14_83-13insA
ENST00000684633.1:n.55-14_55-13insA
ENST00000684678.1:c.79-14_79-13insA	ENSP00000507059.1:n.79-14_79-13insA
ENST00000369842.9:c.83-14_83-13insA MANE Select	ENSP00000358857.4:n.83-14_83-13insA
ENST00000369835.3:c.82+110_82+111insA	ENSP00000358850.3:n.82+110_82+111insA
ENST00000369842.8:c.83-14_83-13insA	ENSP00000358857.4:n.83-14_83-13insA
ENST00000428228.5:c.54-14_54-13insA	ENSP00000401081.1:n.54-14_54-13insA
ENST00000468294.5:n.43-14_43-13insA
ENST00000485261.1:n.163+110_163+111insA
ENST00000486738.5:n.227-14_227-13insA
ENST00000492448.1:n.52_53insA
ENST00000494443.5:n.140-14_140-13insA
NM_000117.2:c.83-14_83-13insA , LRG_745t1:c.83-14_83-13insA	NP_000108.1:n.83-14_83-13insA
XM_024452349.1:c.-126-14_-126-13insA	XP_024308117.1:n.-126-14_-126-13insA
NM_000117.3:c.83-14_83-13insA MANE Select	NP_000108.1:n.83-14_83-13insA