Canonical Allele Identifier: CA916992908

Gene: HGD

Linked Data

• dbSNP Id: rs1559787888

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120646558del , CM000665.2:g.120646558del	GRCh38
NC_000003.11:g.120365405del , CM000665.1:g.120365405del	GRCh37
NC_000003.10:g.121848095del	NCBI36
NG_011957.1:g.40928del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.550-188del MANE Select	ENSP00000283871.5:n.550-188del
ENST00000283871.9:c.550-188del	ENSP00000283871.5:n.550-188del
ENST00000475447.2:c.81-188del
ENST00000492108.5:c.180+419del	ENSP00000419838.1:n.180+419del
NM_000187.3:c.550-188del	NP_000178.2:n.550-188del
XM_005247412.1:c.549+419del	XP_005247469.1:n.549+419del
XM_005247413.1:c.550-188del	XP_005247470.1:n.550-188del
XM_005247414.3:c.550-188del	XP_005247471.1:n.550-188del
XM_011512746.1:c.550-188del	XP_011511048.1:n.550-188del
XM_005247412.2:c.549+419del	XP_005247469.1:n.549+419del
XM_005247413.2:c.550-188del	XP_005247470.1:n.550-188del
XM_005247414.5:c.550-188del	XP_005247471.1:n.550-188del
XM_011512746.2:c.550-188del	XP_011511048.1:n.550-188del
XM_017006277.2:c.127-188del	XP_016861766.1:n.127-188del
NM_000187.4:c.550-188del MANE Select	NP_000178.2:n.550-188del