Canonical Allele Identifier: CA354073257

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120357300A>G (hg19) ; chr3:g.120638453A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120638453A>G , CM000665.2:g.120638453A>G	GRCh38
NC_000003.11:g.120357300A>G , CM000665.1:g.120357300A>G	GRCh37
NC_000003.10:g.121839990A>G	NCBI36
NG_011957.1:g.49029T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.1006+2T>C MANE Select	ENSP00000283871.5:n.1006+2T>C
ENST00000283871.9:c.1006+2T>C	ENSP00000283871.5:n.1006+2T>C
ENST00000470321.1:n.346+2T>C
ENST00000475447.2:c.307+3136T>C
ENST00000492108.5:c.285+3136T>C	ENSP00000419838.1:n.285+3136T>C
ENST00000494453.1:c.426+2T>C
NM_000187.3:c.1006+2T>C	NP_000178.2:n.1006+2T>C
XM_005247412.1:c.781+2T>C	XP_005247469.1:n.781+2T>C
XM_005247413.1:c.1006+2T>C	XP_005247470.1:n.1006+2T>C
XM_011512746.1:c.879+3136T>C	XP_011511048.1:n.879+3136T>C
XM_005247412.2:c.781+2T>C	XP_005247469.1:n.781+2T>C
XM_005247413.2:c.1006+2T>C	XP_005247470.1:n.1006+2T>C
XM_011512746.2:c.879+3136T>C	XP_011511048.1:n.879+3136T>C
XM_017006277.2:c.583+2T>C	XP_016861766.1:n.583+2T>C
NM_000187.4:c.1006+2T>C MANE Select	NP_000178.2:n.1006+2T>C