Canonical Allele Identifier: CA1908701589

Gene: DRGX

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49368631A= , CM000672.2:g.49368631A=	GRCh38
NC_000010.10:g.50576676A= , CM000672.1:g.50576676A=	GRCh37
NC_000010.9:g.50246682A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000374139.8:c.527-2250T= MANE Select	ENSP00000363254.1:n.527-2250T=
ENST00000374139.6:c.527-2250T=	ENSP00000363254.1:n.527-2250T=
ENST00000434016.2:c.527-2250T=	ENSP00000401653.2:n.527-2250T=
NM_001276451.1:c.527-2250T=	NP_001263380.1:n.527-2250T=
XM_011540089.1:c.632-2250T=	XP_011538391.1:n.632-2250T=
XM_011540090.1:c.212-2250T=	XP_011538392.1:n.212-2250T=
XM_011540089.3:c.632-2250T=	XP_011538391.1:n.632-2250T=
NM_001276451.2:c.527-2250T= MANE Select	NP_001263380.1:n.527-2250T=