Canonical Allele Identifier: CA645171834

Gene: EMD

Linked Data

• gnomAD v2: X-153607812-GCCGCCAGGCCT-G
• gnomAD v4: X-154379452-GCCGCCAGGCCT-G
• MyVariant Identifiers: chrX:g.153607813_153607823del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379458_154379468del , CM000685.2:g.154379458_154379468del	GRCh38
NC_000023.10:g.153607818_153607828del , CM000685.1:g.153607818_153607828del	GRCh37
NC_000023.9:g.153261012_153261022del	NCBI36
NG_008677.1:g.10023_10033del , LRG_745:g.10023_10033del
NG_011506.1:g.184_194del
NG_011506.2:g.176_186del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.-27_-17del	ENSP00000507245.1:n.-27_-17del
ENST00000369842.9:c.-27_-17del MANE Select	ENSP00000358857.4:n.-27_-17del
ENST00000369835.3:c.-27_-17del	ENSP00000358850.3:n.-27_-17del
ENST00000369842.8:c.-27_-17del	ENSP00000358857.4:n.-27_-17del
ENST00000428228.5:c.-27_-17del	ENSP00000401081.1:n.-27_-17del
ENST00000485261.1:n.55_65del
ENST00000486738.5:n.118_128del
ENST00000494443.5:n.31_41del
NM_000117.2:c.-27_-17del , LRG_745t1:c.-27_-17del	NP_000108.1:n.-27_-17del
XM_024452349.1:c.-235_-225del	XP_024308117.1:n.-235_-225del
NM_000117.3:c.-27_-17del MANE Select	NP_000108.1:n.-27_-17del