Canonical Allele Identifier: CA360409170

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041503A>C (hg19) ; chr5:g.90745686A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745686A>C , CM000667.2:g.90745686A>C	GRCh38
NC_000005.9:g.90041503A>C , CM000667.1:g.90041503A>C	GRCh37
NC_000005.8:g.90077259A>C	NCBI36
NG_007083.1:g.191887A>C
NG_007083.2:g.221343A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10865A>C MANE Select	ENSP00000384582.2:p.Lys3622Thr
ENST00000639431.1:c.265+69477A>C	ENSP00000491057.1:n.265+69477A>C
ENST00000640374.1:n.4009A>C
ENST00000640464.1:n.1284A>C
ENST00000405460.6:c.10865A>C	ENSP00000384582.2:p.Lys3622Thr
ENST00000509621.1:c.3562A>C
NM_032119.3:c.10865A>C	NP_115495.3:p.Lys3622Thr
NR_003149.1:n.10878A>C
XM_011543675.1:c.10862A>C	XP_011541977.1:p.Lys3621Thr
XM_011543676.1:c.10784A>C	XP_011541978.1:p.Lys3595Thr
XM_011543677.1:c.8168A>C	XP_011541979.1:p.Lys2723Thr
XM_011543678.1:c.10865A>C	XP_011541980.1:p.Lys3622Thr
XM_011543679.1:c.*87A>C	XP_011541981.1:n.*87A>C
NM_032119.4:c.10865A>C MANE Select	NP_115495.3:p.Lys3622Thr
XM_017009963.2:c.10886A>C	XP_016865452.1:p.Lys3629Thr
XM_017009964.2:c.10883A>C	XP_016865453.1:p.Lys3628Thr
XM_017009965.1:c.10883A>C	XP_016865454.1:p.Lys3628Thr
XM_017009966.2:c.10805A>C	XP_016865455.1:p.Lys3602Thr
XM_017009967.1:c.10790A>C	XP_016865456.1:p.Lys3597Thr
XM_017009968.2:c.10886A>C	XP_016865457.1:p.Lys3629Thr
XM_017009969.2:c.10886A>C	XP_016865458.1:p.Lys3629Thr
XM_017009970.2:c.10886A>C	XP_016865459.1:p.Lys3629Thr
XM_017009971.2:c.10886A>C	XP_016865460.1:p.Lys3629Thr
XM_017009972.1:c.4004A>C	XP_016865461.1:p.Lys1335Thr
XM_017009973.1:c.3983A>C	XP_016865462.1:p.Lys1328Thr
XM_017009974.2:c.*87A>C	XP_016865463.1:n.*87A>C
NR_003149.2:n.10881A>C