Canonical Allele Identifier: CA915941091
Gene: CHM HGNC NCBI

Linked Data

ClinVar Variation Id: 812270
ClinVar RCV Id: RCV001002949

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.85963667_85964054del , CM000685.2:g.85963667_85964054del GRCh38
NC_000023.10:g.85218672_85219059del , CM000685.1:g.85218672_85219059del GRCh37
NC_000023.9:g.85105328_85105715del NCBI36
NG_009874.2:g.88511_88898del , LRG_699:g.88511_88898del

Transcript Alleles

HGVS Amino-acid change
ENST00000357749.7:c.315_702del
ENST00000357749.6:c.315_702del
ENST00000467744.2:n.126+63439_126+63826del
NM_000390.2:c.315_702del , LRG_699t1:c.315_702del
XM_006724615.2:c.252_639del
XM_011530839.1:c.-130_258del
NM_000390.3:c.315_702del
NM_001320959.1:c.-130_258del
NM_001362517.1:c.-130_258del
NM_001362518.1:c.-126-4_258del
NM_001362519.1:c.-126-4_258del
XM_017029242.2:c.315_702del
XM_017029246.1:c.-126-4_258del
XM_024452331.1:c.-130_258del
NM_000390.4:c.315_702del
NM_001362518.2:c.-126-4_258del