Canonical Allele Identifier: CA2580936346
Gene: DRGX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49368588C>A , CM000672.2:g.49368588C>A GRCh38
NC_000010.10:g.50576633C>A , CM000672.1:g.50576633C>A GRCh37
NC_000010.9:g.50246639C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374139.8:c.527-2207G>T MANE Select ENSP00000363254.1:n.527-2207G>T
ENST00000374139.6:c.527-2207G>T ENSP00000363254.1:n.527-2207G>T
ENST00000434016.2:c.527-2207G>T ENSP00000401653.2:n.527-2207G>T
NM_001276451.1:c.527-2207G>T NP_001263380.1:n.527-2207G>T
XM_011540089.1:c.632-2207G>T XP_011538391.1:n.632-2207G>T
XM_011540090.1:c.212-2207G>T XP_011538392.1:n.212-2207G>T
XM_011540089.3:c.632-2207G>T XP_011538391.1:n.632-2207G>T
NM_001276451.2:c.527-2207G>T MANE Select NP_001263380.1:n.527-2207G>T