Canonical Allele Identifier: CA360410720

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106823G>T (hg19) ; chr5:g.90811006G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811006G>T , CM000667.2:g.90811006G>T	GRCh38
NC_000005.9:g.90106823G>T , CM000667.1:g.90106823G>T	GRCh37
NC_000005.8:g.90142579G>T	NCBI36
NG_007083.1:g.257207G>T
NG_007083.2:g.286663G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15746G>T MANE Select	ENSP00000384582.2:p.Gly5249Val
ENST00000425867.3:c.4700G>T	ENSP00000392618.3:p.Gly1567Val
ENST00000638510.1:n.3013G>T
ENST00000639431.1:c.265+134797G>T	ENSP00000491057.1:n.265+134797G>T
ENST00000640407.1:c.2156G>T	ENSP00000491425.1:p.Gly719Val
ENST00000405460.6:c.15746G>T	ENSP00000384582.2:p.Gly5249Val
ENST00000425867.2:c.2729G>T	ENSP00000392618.2:p.Gly910Val
NM_032119.3:c.15746G>T	NP_115495.3:p.Gly5249Val
NR_003149.1:n.15759G>T
XM_011543675.1:c.15743G>T	XP_011541977.1:p.Gly5248Val
XM_011543676.1:c.15665G>T	XP_011541978.1:p.Gly5222Val
XM_011543677.1:c.13049G>T	XP_011541979.1:p.Gly4350Val
NM_032119.4:c.15746G>T MANE Select	NP_115495.3:p.Gly5249Val
XM_017009963.2:c.15767G>T	XP_016865452.1:p.Gly5256Val
XM_017009964.2:c.15764G>T	XP_016865453.1:p.Gly5255Val
XM_017009965.1:c.15764G>T	XP_016865454.1:p.Gly5255Val
XM_017009966.2:c.15686G>T	XP_016865455.1:p.Gly5229Val
XM_017009967.1:c.15671G>T	XP_016865456.1:p.Gly5224Val
XM_017009968.2:c.15587G>T	XP_016865457.1:p.Gly5196Val
XM_017009969.2:c.15767G>T	XP_016865458.1:p.Gly5256Val
XM_017009972.1:c.8885G>T	XP_016865461.1:p.Gly2962Val
XM_017009973.1:c.8864G>T	XP_016865462.1:p.Gly2955Val
NR_003149.2:n.15762G>T