Canonical Allele Identifier: CA2466663824
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379694A= , CM000685.2:g.154379694A= GRCh38
NC_000023.10:g.153608054A= , CM000685.1:g.153608054A= GRCh37
NC_000023.9:g.153261248A= NCBI36
NG_008677.1:g.10259A= , LRG_745:g.10259A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.87A= ENSP00000507245.1:p.Ser29=
ENST00000682478.1:n.63A=
ENST00000683576.1:n.63A=
ENST00000683627.1:c.87A= ENSP00000507533.1:p.Ser29=
ENST00000684082.1:c.87A= ENSP00000508266.1:p.Ser29=
ENST00000684633.1:n.59A=
ENST00000684678.1:c.83A= ENSP00000507059.1:p.Gln28=
ENST00000369842.9:c.87A= MANE Select ENSP00000358857.4:p.Ser29=
ENST00000369835.3:c.82+128A= ENSP00000358850.3:n.82+128A=
ENST00000369842.8:c.87A= ENSP00000358857.4:p.Ser29=
ENST00000428228.5:c.58A= ENSP00000401081.1:p.Asn20=
ENST00000468294.5:n.47A=
ENST00000485261.1:n.163+128A=
ENST00000486738.5:n.231A=
ENST00000492448.1:n.70A=
ENST00000494443.5:n.144A=
NM_000117.2:c.87A= , LRG_745t1:c.87A= NP_000108.1:p.Ser29=
XM_024452349.1:c.-122A= XP_024308117.1:n.-122A=
NM_000117.3:c.87A= MANE Select NP_000108.1:p.Ser29=