Canonical Allele Identifier: CA445411970

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712373-T-C
• MyVariant Identifiers: chr5:g.90008190T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712373T>C , CM000667.2:g.90712373T>C	GRCh38
NC_000005.9:g.90008190T>C , CM000667.1:g.90008190T>C	GRCh37
NC_000005.8:g.90043946T>C	NCBI36
NG_007083.1:g.158574T>C
NG_007083.2:g.188030T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9129T>C MANE Select	ENSP00000384582.2:p.Phe3043=
ENST00000639431.1:c.265+36164T>C	ENSP00000491057.1:n.265+36164T>C
ENST00000639473.1:n.4588T>C
ENST00000640012.1:c.2936T>C
ENST00000640374.1:n.2273T>C
ENST00000640779.1:c.3858T>C
ENST00000405460.6:c.9129T>C	ENSP00000384582.2:p.Phe3043=
ENST00000509621.1:c.1826T>C
NM_032119.3:c.9129T>C	NP_115495.3:p.Phe3043=
NR_003149.1:n.9142T>C
XM_011543675.1:c.9126T>C	XP_011541977.1:p.Phe3042=
XM_011543676.1:c.9048T>C	XP_011541978.1:p.Phe3016=
XM_011543677.1:c.6432T>C	XP_011541979.1:p.Phe2144=
XM_011543678.1:c.9129T>C	XP_011541980.1:p.Phe3043=
XM_011543679.1:c.9129T>C	XP_011541981.1:p.Phe3043=
NM_032119.4:c.9129T>C MANE Select	NP_115495.3:p.Phe3043=
XM_017009963.2:c.9150T>C	XP_016865452.1:p.Phe3050=
XM_017009964.2:c.9147T>C	XP_016865453.1:p.Phe3049=
XM_017009965.1:c.9147T>C	XP_016865454.1:p.Phe3049=
XM_017009966.2:c.9069T>C	XP_016865455.1:p.Phe3023=
XM_017009967.1:c.9054T>C	XP_016865456.1:p.Phe3018=
XM_017009968.2:c.9150T>C	XP_016865457.1:p.Phe3050=
XM_017009969.2:c.9150T>C	XP_016865458.1:p.Phe3050=
XM_017009970.2:c.9150T>C	XP_016865459.1:p.Phe3050=
XM_017009971.2:c.9150T>C	XP_016865460.1:p.Phe3050=
XM_017009972.1:c.2268T>C	XP_016865461.1:p.Phe756=
XM_017009973.1:c.2247T>C	XP_016865462.1:p.Phe749=
XM_017009974.2:c.9150T>C	XP_016865463.1:p.Phe3050=
NR_003149.2:n.9145T>C