Canonical Allele Identifier: CA445413828

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012477C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716660C>G , CM000667.2:g.90716660C>G	GRCh38
NC_000005.9:g.90012477C>G , CM000667.1:g.90012477C>G	GRCh37
NC_000005.8:g.90048233C>G	NCBI36
NG_007083.1:g.162861C>G
NG_007083.2:g.192317C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9378C>G MANE Select	ENSP00000384582.2:p.Ser3126=
ENST00000639431.1:c.265+40451C>G	ENSP00000491057.1:n.265+40451C>G
ENST00000639473.1:n.4837C>G
ENST00000640012.1:c.3185C>G
ENST00000640374.1:n.2522C>G
ENST00000640779.1:c.4107C>G
ENST00000405460.6:c.9378C>G	ENSP00000384582.2:p.Ser3126=
ENST00000509621.1:c.2075C>G
NM_032119.3:c.9378C>G	NP_115495.3:p.Ser3126=
NR_003149.1:n.9391C>G
XM_011543675.1:c.9375C>G	XP_011541977.1:p.Ser3125=
XM_011543676.1:c.9297C>G	XP_011541978.1:p.Ser3099=
XM_011543677.1:c.6681C>G	XP_011541979.1:p.Ser2227=
XM_011543678.1:c.9378C>G	XP_011541980.1:p.Ser3126=
XM_011543679.1:c.9378C>G	XP_011541981.1:p.Ser3126=
XR_948560.1:n.272-851G>C
NM_032119.4:c.9378C>G MANE Select	NP_115495.3:p.Ser3126=
XM_017009963.2:c.9399C>G	XP_016865452.1:p.Ser3133=
XM_017009964.2:c.9396C>G	XP_016865453.1:p.Ser3132=
XM_017009965.1:c.9396C>G	XP_016865454.1:p.Ser3132=
XM_017009966.2:c.9318C>G	XP_016865455.1:p.Ser3106=
XM_017009967.1:c.9303C>G	XP_016865456.1:p.Ser3101=
XM_017009968.2:c.9399C>G	XP_016865457.1:p.Ser3133=
XM_017009969.2:c.9399C>G	XP_016865458.1:p.Ser3133=
XM_017009970.2:c.9399C>G	XP_016865459.1:p.Ser3133=
XM_017009971.2:c.9399C>G	XP_016865460.1:p.Ser3133=
XM_017009972.1:c.2517C>G	XP_016865461.1:p.Ser839=
XM_017009973.1:c.2496C>G	XP_016865462.1:p.Ser832=
XM_017009974.2:c.9399C>G	XP_016865463.1:p.Ser3133=
XR_001742802.1:n.2523-851G>C
NR_003149.2:n.9394C>G