Canonical Allele Identifier: CA1397093030

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120638382_120638383delinsTC , CM000665.2:g.120638382_120638383delinsTC	GRCh38
NC_000003.11:g.120357229_120357230delinsTC , CM000665.1:g.120357229_120357230delinsTC	GRCh37
NC_000003.10:g.121839919_121839920delinsTC	NCBI36
NG_011957.1:g.49099_49100delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.1006+72_1006+73delinsGA MANE Select	ENSP00000283871.5:n.1006+72_1006+73delinsGA
ENST00000283871.9:c.1006+72_1006+73delinsGA	ENSP00000283871.5:n.1006+72_1006+73delinsGA
ENST00000470321.1:n.346+72_346+73delinsGA
ENST00000475447.2:c.307+3206_307+3207delinsGA
ENST00000492108.5:c.285+3206_285+3207delinsGA	ENSP00000419838.1:n.285+3206_285+3207delinsGA
ENST00000494453.1:c.426+72_426+73delinsGA
NM_000187.3:c.1006+72_1006+73delinsGA	NP_000178.2:n.1006+72_1006+73delinsGA
XM_005247412.1:c.781+72_781+73delinsGA	XP_005247469.1:n.781+72_781+73delinsGA
XM_005247413.1:c.1006+72_1006+73delinsGA	XP_005247470.1:n.1006+72_1006+73delinsGA
XM_011512746.1:c.879+3206_879+3207delinsGA	XP_011511048.1:n.879+3206_879+3207delinsGA
XM_005247412.2:c.781+72_781+73delinsGA	XP_005247469.1:n.781+72_781+73delinsGA
XM_005247413.2:c.1006+72_1006+73delinsGA	XP_005247470.1:n.1006+72_1006+73delinsGA
XM_011512746.2:c.879+3206_879+3207delinsGA	XP_011511048.1:n.879+3206_879+3207delinsGA
XM_017006277.2:c.583+72_583+73delinsGA	XP_016861766.1:n.583+72_583+73delinsGA
NM_000187.4:c.1006+72_1006+73delinsGA MANE Select	NP_000178.2:n.1006+72_1006+73delinsGA