Canonical Allele Identifier: CA415258684

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609315A>C (hg19) ; chrX:g.154380955A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380955A>C , CM000685.2:g.154380955A>C	GRCh38
NC_000023.10:g.153609315A>C , CM000685.1:g.153609315A>C	GRCh37
NC_000023.9:g.153262509A>C	NCBI36
NG_008677.1:g.11520A>C , LRG_745:g.11520A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.523A>C	ENSP00000507245.1:p.Ser175Arg
ENST00000682478.1:n.713A>C
ENST00000683576.1:n.713A>C
ENST00000683627.1:c.523A>C	ENSP00000507533.1:p.Ser175Arg
ENST00000684082.1:c.480A>C	ENSP00000508266.1:n.480A>C
ENST00000684633.1:n.495A>C
ENST00000684678.1:c.519A>C	ENSP00000507059.1:n.519A>C
ENST00000369842.9:c.523A>C MANE Select	ENSP00000358857.4:p.Ser175Arg
ENST00000369835.3:c.418A>C	ENSP00000358850.3:p.Ser140Arg
ENST00000369842.8:c.523A>C	ENSP00000358857.4:p.Ser175Arg
ENST00000428228.5:c.*428A>C	ENSP00000401081.1:n.*428A>C
ENST00000471965.1:n.312A>C
ENST00000485261.1:n.792A>C
ENST00000486738.5:n.960A>C
ENST00000492448.1:n.506A>C
NM_000117.2:c.523A>C , LRG_745t1:c.523A>C	NP_000108.1:p.Ser175Arg
XM_024452349.1:c.529A>C	XP_024308117.1:p.Ser177Arg
NM_000117.3:c.523A>C MANE Select	NP_000108.1:p.Ser175Arg