Canonical Allele Identifier: CA360396280

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008177G>C (hg19) ; chr5:g.90712360G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712360G>C , CM000667.2:g.90712360G>C	GRCh38
NC_000005.9:g.90008177G>C , CM000667.1:g.90008177G>C	GRCh37
NC_000005.8:g.90043933G>C	NCBI36
NG_007083.1:g.158561G>C
NG_007083.2:g.188017G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9116G>C MANE Select	ENSP00000384582.2:p.Gly3039Ala
ENST00000639431.1:c.265+36151G>C	ENSP00000491057.1:n.265+36151G>C
ENST00000639473.1:n.4575G>C
ENST00000640012.1:c.2923G>C
ENST00000640374.1:n.2260G>C
ENST00000640779.1:c.3845G>C
ENST00000405460.6:c.9116G>C	ENSP00000384582.2:p.Gly3039Ala
ENST00000509621.1:c.1813G>C
NM_032119.3:c.9116G>C	NP_115495.3:p.Gly3039Ala
NR_003149.1:n.9129G>C
XM_011543675.1:c.9113G>C	XP_011541977.1:p.Gly3038Ala
XM_011543676.1:c.9035G>C	XP_011541978.1:p.Gly3012Ala
XM_011543677.1:c.6419G>C	XP_011541979.1:p.Gly2140Ala
XM_011543678.1:c.9116G>C	XP_011541980.1:p.Gly3039Ala
XM_011543679.1:c.9116G>C	XP_011541981.1:p.Gly3039Ala
NM_032119.4:c.9116G>C MANE Select	NP_115495.3:p.Gly3039Ala
XM_017009963.2:c.9137G>C	XP_016865452.1:p.Gly3046Ala
XM_017009964.2:c.9134G>C	XP_016865453.1:p.Gly3045Ala
XM_017009965.1:c.9134G>C	XP_016865454.1:p.Gly3045Ala
XM_017009966.2:c.9056G>C	XP_016865455.1:p.Gly3019Ala
XM_017009967.1:c.9041G>C	XP_016865456.1:p.Gly3014Ala
XM_017009968.2:c.9137G>C	XP_016865457.1:p.Gly3046Ala
XM_017009969.2:c.9137G>C	XP_016865458.1:p.Gly3046Ala
XM_017009970.2:c.9137G>C	XP_016865459.1:p.Gly3046Ala
XM_017009971.2:c.9137G>C	XP_016865460.1:p.Gly3046Ala
XM_017009972.1:c.2255G>C	XP_016865461.1:p.Gly752Ala
XM_017009973.1:c.2234G>C	XP_016865462.1:p.Gly745Ala
XM_017009974.2:c.9137G>C	XP_016865463.1:p.Gly3046Ala
NR_003149.2:n.9132G>C