Canonical Allele Identifier: CA2466663828
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379715G= , CM000685.2:g.154379715G= GRCh38
NC_000023.10:g.153608075G= , CM000685.1:g.153608075G= GRCh37
NC_000023.9:g.153261269G= NCBI36
NG_008677.1:g.10280G= , LRG_745:g.10280G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682114.1:c.108G= ENSP00000507245.1:p.Lys36=
ENST00000682478.1:n.84G=
ENST00000683576.1:n.84G=
ENST00000683627.1:c.108G= ENSP00000507533.1:p.Lys36=
ENST00000684082.1:c.108G= ENSP00000508266.1:p.Lys36=
ENST00000684633.1:n.80G=
ENST00000684678.1:c.104G= ENSP00000507059.1:p.Arg35=
ENST00000369842.9:c.108G= MANE Select ENSP00000358857.4:p.Lys36=
ENST00000369835.3:c.82+149G= ENSP00000358850.3:n.82+149G=
ENST00000369842.8:c.108G= ENSP00000358857.4:p.Lys36=
ENST00000428228.5:c.*13G= ENSP00000401081.1:n.*13G=
ENST00000468294.5:n.68G=
ENST00000485261.1:n.163+149G=
ENST00000486738.5:n.252G=
ENST00000492448.1:n.91G=
ENST00000494443.5:n.165G=
NM_000117.2:c.108G= , LRG_745t1:c.108G= NP_000108.1:p.Lys36=
XM_024452349.1:c.-101G= XP_024308117.1:n.-101G=
NM_000117.3:c.108G= MANE Select NP_000108.1:p.Lys36=