Canonical Allele Identifier: CA10527182

Gene: ADGRG4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136399888C>G , CM000685.2:g.136399888C>G	GRCh38
NC_000023.10:g.135482047C>G , CM000685.1:g.135482047C>G	GRCh37
NC_000023.9:g.135309713C>G	NCBI36
NG_021219.1:g.103926C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394143.6:c.8347C>G MANE Select	ENSP00000377699.1:p.Leu2783Val
ENST00000370652.5:c.8347C>G	ENSP00000359686.1:p.Leu2783Val
ENST00000394141.1:c.7732C>G	ENSP00000377697.1:p.Leu2578Val
ENST00000394143.5:c.8347C>G	ENSP00000377699.1:p.Leu2783Val
NM_153834.3:c.8347C>G	NP_722576.3:p.Leu2783Val
XM_011531268.1:c.8347C>G	XP_011529570.1:p.Leu2783Val
XM_011531269.1:c.8347C>G	XP_011529571.1:p.Leu2783Val
XM_011531270.1:c.8212C>G	XP_011529572.1:p.Leu2738Val
XM_011531271.1:c.8158C>G	XP_011529573.1:p.Leu2720Val
XM_011531272.1:c.8225C>G	XP_011529574.1:p.Pro2742Arg
XM_011531269.2:c.8347C>G	XP_011529571.1:p.Leu2783Val
XM_011531271.2:c.8158C>G	XP_011529573.1:p.Leu2720Val
NM_153834.4:c.8347C>G MANE Select	NP_722576.3:p.Leu2783Val