Canonical Allele Identifier: CA445416065

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041459A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745642A>C , CM000667.2:g.90745642A>C	GRCh38
NC_000005.9:g.90041459A>C , CM000667.1:g.90041459A>C	GRCh37
NC_000005.8:g.90077215A>C	NCBI36
NG_007083.1:g.191843A>C
NG_007083.2:g.221299A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10821A>C MANE Select	ENSP00000384582.2:p.Val3607=
ENST00000639431.1:c.265+69433A>C	ENSP00000491057.1:n.265+69433A>C
ENST00000640374.1:n.3965A>C
ENST00000640464.1:n.1240A>C
ENST00000405460.6:c.10821A>C	ENSP00000384582.2:p.Val3607=
ENST00000509621.1:c.3518A>C
NM_032119.3:c.10821A>C	NP_115495.3:p.Val3607=
NR_003149.1:n.10834A>C
XM_011543675.1:c.10818A>C	XP_011541977.1:p.Val3606=
XM_011543676.1:c.10740A>C	XP_011541978.1:p.Val3580=
XM_011543677.1:c.8124A>C	XP_011541979.1:p.Val2708=
XM_011543678.1:c.10821A>C	XP_011541980.1:p.Val3607=
XM_011543679.1:c.*43A>C	XP_011541981.1:n.*43A>C
NM_032119.4:c.10821A>C MANE Select	NP_115495.3:p.Val3607=
XM_017009963.2:c.10842A>C	XP_016865452.1:p.Val3614=
XM_017009964.2:c.10839A>C	XP_016865453.1:p.Val3613=
XM_017009965.1:c.10839A>C	XP_016865454.1:p.Val3613=
XM_017009966.2:c.10761A>C	XP_016865455.1:p.Val3587=
XM_017009967.1:c.10746A>C	XP_016865456.1:p.Val3582=
XM_017009968.2:c.10842A>C	XP_016865457.1:p.Val3614=
XM_017009969.2:c.10842A>C	XP_016865458.1:p.Val3614=
XM_017009970.2:c.10842A>C	XP_016865459.1:p.Val3614=
XM_017009971.2:c.10842A>C	XP_016865460.1:p.Val3614=
XM_017009972.1:c.3960A>C	XP_016865461.1:p.Val1320=
XM_017009973.1:c.3939A>C	XP_016865462.1:p.Val1313=
XM_017009974.2:c.*43A>C	XP_016865463.1:n.*43A>C
NR_003149.2:n.10837A>C