Canonical Allele Identifier: CA16608835
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 393234
ClinVar RCV Id: RCV000441327
dbSNP Id: rs1057524848

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380772T>A , CM000685.2:g.154380772T>A GRCh38
NC_000023.10:g.153609132T>A , CM000685.1:g.153609132T>A GRCh37
NC_000023.9:g.153262326T>A NCBI36
NG_008677.1:g.11337T>A , LRG_745:g.11337T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.419T>A ENSP00000507245.1:p.Leu140Ter
ENST00000682478.1:n.609T>A
ENST00000683576.1:n.609T>A
ENST00000683627.1:c.419T>A ENSP00000507533.1:p.Leu140Ter
ENST00000684082.1:c.376T>A ENSP00000508266.1:n.376T>A
ENST00000684633.1:n.391T>A
ENST00000684678.1:c.415T>A ENSP00000507059.1:n.415T>A
ENST00000369842.9:c.419T>A MANE Select ENSP00000358857.4:p.Leu140Ter
ENST00000369835.3:c.314T>A ENSP00000358850.3:p.Leu105Ter
ENST00000369842.8:c.419T>A ENSP00000358857.4:p.Leu140Ter
ENST00000428228.5:c.*324T>A ENSP00000401081.1:n.*324T>A
ENST00000468294.5:n.379T>A
ENST00000471965.1:n.208T>A
ENST00000485261.1:n.609T>A
ENST00000486738.5:n.777T>A
ENST00000492448.1:n.402T>A
NM_000117.2:c.419T>A , LRG_745t1:c.419T>A NP_000108.1:p.Leu140Ter
XM_024452349.1:c.425T>A XP_024308117.1:p.Leu142Ter
NM_000117.3:c.419T>A MANE Select NP_000108.1:p.Leu140Ter