Canonical Allele Identifier: CA10561619
Gene: EMD HGNC NCBI

Linked Data

dbSNP Id: rs781943158

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380890C>T , CM000685.2:g.154380890C>T GRCh38
NC_000023.10:g.153609250C>T , CM000685.1:g.153609250C>T GRCh37
NC_000023.9:g.153262444C>T NCBI36
NG_008677.1:g.11455C>T , LRG_745:g.11455C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.458C>T ENSP00000507245.1:p.Pro153Leu
ENST00000682478.1:n.648C>T
ENST00000683576.1:n.648C>T
ENST00000683627.1:c.458C>T ENSP00000507533.1:p.Pro153Leu
ENST00000684082.1:c.415C>T ENSP00000508266.1:n.415C>T
ENST00000684633.1:n.430C>T
ENST00000684678.1:c.454C>T ENSP00000507059.1:n.454C>T
ENST00000369842.9:c.458C>T MANE Select ENSP00000358857.4:p.Pro153Leu
ENST00000369835.3:c.353C>T ENSP00000358850.3:p.Pro118Leu
ENST00000369842.8:c.458C>T ENSP00000358857.4:p.Pro153Leu
ENST00000428228.5:c.*363C>T ENSP00000401081.1:n.*363C>T
ENST00000468294.5:n.497C>T
ENST00000471965.1:n.247C>T
ENST00000485261.1:n.727C>T
ENST00000486738.5:n.895C>T
ENST00000492448.1:n.441C>T
NM_000117.2:c.458C>T , LRG_745t1:c.458C>T NP_000108.1:p.Pro153Leu
XM_024452349.1:c.464C>T XP_024308117.1:p.Pro155Leu
NM_000117.3:c.458C>T MANE Select NP_000108.1:p.Pro153Leu