Canonical Allele Identifier: CA445413837

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012480A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716663A>G , CM000667.2:g.90716663A>G	GRCh38
NC_000005.9:g.90012480A>G , CM000667.1:g.90012480A>G	GRCh37
NC_000005.8:g.90048236A>G	NCBI36
NG_007083.1:g.162864A>G
NG_007083.2:g.192320A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9381A>G MANE Select	ENSP00000384582.2:p.Ser3127=
ENST00000639431.1:c.265+40454A>G	ENSP00000491057.1:n.265+40454A>G
ENST00000639473.1:n.4840A>G
ENST00000640012.1:c.3188A>G
ENST00000640374.1:n.2525A>G
ENST00000640779.1:c.4110A>G
ENST00000405460.6:c.9381A>G	ENSP00000384582.2:p.Ser3127=
ENST00000509621.1:c.2078A>G
NM_032119.3:c.9381A>G	NP_115495.3:p.Ser3127=
NR_003149.1:n.9394A>G
XM_011543675.1:c.9378A>G	XP_011541977.1:p.Ser3126=
XM_011543676.1:c.9300A>G	XP_011541978.1:p.Ser3100=
XM_011543677.1:c.6684A>G	XP_011541979.1:p.Ser2228=
XM_011543678.1:c.9381A>G	XP_011541980.1:p.Ser3127=
XM_011543679.1:c.9381A>G	XP_011541981.1:p.Ser3127=
XR_948560.1:n.272-854T>C
NM_032119.4:c.9381A>G MANE Select	NP_115495.3:p.Ser3127=
XM_017009963.2:c.9402A>G	XP_016865452.1:p.Ser3134=
XM_017009964.2:c.9399A>G	XP_016865453.1:p.Ser3133=
XM_017009965.1:c.9399A>G	XP_016865454.1:p.Ser3133=
XM_017009966.2:c.9321A>G	XP_016865455.1:p.Ser3107=
XM_017009967.1:c.9306A>G	XP_016865456.1:p.Ser3102=
XM_017009968.2:c.9402A>G	XP_016865457.1:p.Ser3134=
XM_017009969.2:c.9402A>G	XP_016865458.1:p.Ser3134=
XM_017009970.2:c.9402A>G	XP_016865459.1:p.Ser3134=
XM_017009971.2:c.9402A>G	XP_016865460.1:p.Ser3134=
XM_017009972.1:c.2520A>G	XP_016865461.1:p.Ser840=
XM_017009973.1:c.2499A>G	XP_016865462.1:p.Ser833=
XM_017009974.2:c.9402A>G	XP_016865463.1:p.Ser3134=
XR_001742802.1:n.2523-854T>C
NR_003149.2:n.9397A>G