Canonical Allele Identifier: CA415259127

Gene: EMD

Linked Data

• gnomAD v4: X-154381090-G-T
• MyVariant Identifiers: chrX:g.153609450G>T (hg19) ; chrX:g.154381090G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154381090G>T , CM000685.2:g.154381090G>T	GRCh38
NC_000023.10:g.153609450G>T , CM000685.1:g.153609450G>T	GRCh37
NC_000023.9:g.153262644G>T	NCBI36
NG_008677.1:g.11655G>T , LRG_745:g.11655G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.572+86G>T	ENSP00000507245.1:n.572+86G>T
ENST00000682478.1:n.762+86G>T
ENST00000683576.1:n.848G>T
ENST00000683627.1:c.658G>T	ENSP00000507533.1:p.Asp220Tyr
ENST00000684082.1:c.615G>T	ENSP00000508266.1:n.615G>T
ENST00000684633.1:n.630G>T
ENST00000684678.1:c.568+86G>T	ENSP00000507059.1:n.568+86G>T
ENST00000369842.9:c.658G>T MANE Select	ENSP00000358857.4:p.Asp220Tyr
ENST00000369835.3:c.553G>T	ENSP00000358850.3:p.Asp185Tyr
ENST00000369842.8:c.658G>T	ENSP00000358857.4:p.Asp220Tyr
ENST00000428228.5:c.*563G>T	ENSP00000401081.1:n.*563G>T
ENST00000471965.1:n.447G>T
ENST00000486738.5:n.1095G>T
ENST00000492448.1:n.641G>T
NM_000117.2:c.658G>T , LRG_745t1:c.658G>T	NP_000108.1:p.Asp220Tyr
XM_024452349.1:c.664G>T	XP_024308117.1:p.Asp222Tyr
NM_000117.3:c.658G>T MANE Select	NP_000108.1:p.Asp220Tyr