Canonical Allele Identifier: CA519710057

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609377A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154381017A>C , CM000685.2:g.154381017A>C	GRCh38
NC_000023.10:g.153609377A>C , CM000685.1:g.153609377A>C	GRCh37
NC_000023.9:g.153262571A>C	NCBI36
NG_008677.1:g.11582A>C , LRG_745:g.11582A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.572+13A>C	ENSP00000507245.1:n.572+13A>C
ENST00000682478.1:n.762+13A>C
ENST00000683576.1:n.775A>C
ENST00000683627.1:c.585A>C	ENSP00000507533.1:p.Ser195=
ENST00000684082.1:c.542A>C	ENSP00000508266.1:n.542A>C
ENST00000684633.1:n.557A>C
ENST00000684678.1:c.568+13A>C	ENSP00000507059.1:n.568+13A>C
ENST00000369842.9:c.585A>C MANE Select	ENSP00000358857.4:p.Ser195=
ENST00000369835.3:c.480A>C	ENSP00000358850.3:p.Ser160=
ENST00000369842.8:c.585A>C	ENSP00000358857.4:p.Ser195=
ENST00000428228.5:c.*490A>C	ENSP00000401081.1:n.*490A>C
ENST00000471965.1:n.374A>C
ENST00000486738.5:n.1022A>C
ENST00000492448.1:n.568A>C
NM_000117.2:c.585A>C , LRG_745t1:c.585A>C	NP_000108.1:p.Ser195=
XM_024452349.1:c.591A>C	XP_024308117.1:p.Ser197=
NM_000117.3:c.585A>C MANE Select	NP_000108.1:p.Ser195=