Canonical Allele Identifier: CA415257495

Gene: EMD

Linked Data

• dbSNP Id: rs2067875443
• COSMIC: COSM3559742
• MyVariant Identifiers: chrX:g.153608118C>T (hg19) ; chrX:g.154379758C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379758C>T , CM000685.2:g.154379758C>T	GRCh38
NC_000023.10:g.153608118C>T , CM000685.1:g.153608118C>T	GRCh37
NC_000023.9:g.153261312C>T	NCBI36
NG_008677.1:g.10323C>T , LRG_745:g.10323C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.151C>T	ENSP00000507245.1:p.Pro51Ser
ENST00000682478.1:n.127C>T
ENST00000683576.1:n.127C>T
ENST00000683627.1:c.151C>T	ENSP00000507533.1:p.Pro51Ser
ENST00000684082.1:c.151C>T	ENSP00000508266.1:p.Pro51Ser
ENST00000684633.1:n.123C>T
ENST00000684678.1:c.147C>T	ENSP00000507059.1:p.Pro49=
ENST00000369842.9:c.151C>T MANE Select	ENSP00000358857.4:p.Pro51Ser
ENST00000369835.3:c.83-184C>T	ENSP00000358850.3:n.83-184C>T
ENST00000369842.8:c.151C>T	ENSP00000358857.4:p.Pro51Ser
ENST00000428228.5:c.*56C>T	ENSP00000401081.1:n.*56C>T
ENST00000468294.5:n.111C>T
ENST00000485261.1:n.164-184C>T
ENST00000486738.5:n.295C>T
ENST00000492448.1:n.134C>T
ENST00000494443.5:n.208C>T
NM_000117.2:c.151C>T , LRG_745t1:c.151C>T	NP_000108.1:p.Pro51Ser
XM_024452349.1:c.-58C>T	XP_024308117.1:n.-58C>T
NM_000117.3:c.151C>T MANE Select	NP_000108.1:p.Pro51Ser