Canonical Allele Identifier: CA5739273

Gene: DHX32 BCCIP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125852649A>G , CM000672.2:g.125852649A>G	GRCh38
NC_000010.10:g.127541218A>G , CM000672.1:g.127541218A>G	GRCh37
NC_000010.9:g.127531208A>G	NCBI36
NG_029095.1:g.34115A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_018180.3:c.1093-7T>C (DHX32) MANE Select	NP_060650.2:n.1093-7T>C
ENST00000284690.4:c.1093-7T>C (DHX32) MANE Select	ENSP00000284690.3:n.1093-7T>C
NM_016567.3:c.851-476A>G (BCCIP)	NP_057651.1:n.851-476A>G
NM_016567.4:c.851-476A>G (BCCIP)	NP_057651.1:n.851-476A>G
NM_018180.2:c.1093-7T>C (DHX32)	NP_060650.2:n.1093-7T>C
ENST00000284690.3:c.1093-7T>C (DHX32)	ENSP00000284690.3:n.1093-7T>C
ENST00000368721.5:c.-36-7T>C (DHX32)	ENSP00000357710.1:n.-36-7T>C
ENST00000368759.5:c.851-476A>G (BCCIP)	ENSP00000357748.5:n.851-476A>G