Canonical Allele Identifier: CA360409061

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041478G>C (hg19) ; chr5:g.90745661G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745661G>C , CM000667.2:g.90745661G>C	GRCh38
NC_000005.9:g.90041478G>C , CM000667.1:g.90041478G>C	GRCh37
NC_000005.8:g.90077234G>C	NCBI36
NG_007083.1:g.191862G>C
NG_007083.2:g.221318G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10840G>C MANE Select	ENSP00000384582.2:p.Val3614Leu
ENST00000639431.1:c.265+69452G>C	ENSP00000491057.1:n.265+69452G>C
ENST00000640374.1:n.3984G>C
ENST00000640464.1:n.1259G>C
ENST00000405460.6:c.10840G>C	ENSP00000384582.2:p.Val3614Leu
ENST00000509621.1:c.3537G>C
NM_032119.3:c.10840G>C	NP_115495.3:p.Val3614Leu
NR_003149.1:n.10853G>C
XM_011543675.1:c.10837G>C	XP_011541977.1:p.Val3613Leu
XM_011543676.1:c.10759G>C	XP_011541978.1:p.Val3587Leu
XM_011543677.1:c.8143G>C	XP_011541979.1:p.Val2715Leu
XM_011543678.1:c.10840G>C	XP_011541980.1:p.Val3614Leu
XM_011543679.1:c.*62G>C	XP_011541981.1:n.*62G>C
NM_032119.4:c.10840G>C MANE Select	NP_115495.3:p.Val3614Leu
XM_017009963.2:c.10861G>C	XP_016865452.1:p.Val3621Leu
XM_017009964.2:c.10858G>C	XP_016865453.1:p.Val3620Leu
XM_017009965.1:c.10858G>C	XP_016865454.1:p.Val3620Leu
XM_017009966.2:c.10780G>C	XP_016865455.1:p.Val3594Leu
XM_017009967.1:c.10765G>C	XP_016865456.1:p.Val3589Leu
XM_017009968.2:c.10861G>C	XP_016865457.1:p.Val3621Leu
XM_017009969.2:c.10861G>C	XP_016865458.1:p.Val3621Leu
XM_017009970.2:c.10861G>C	XP_016865459.1:p.Val3621Leu
XM_017009971.2:c.10861G>C	XP_016865460.1:p.Val3621Leu
XM_017009972.1:c.3979G>C	XP_016865461.1:p.Val1327Leu
XM_017009973.1:c.3958G>C	XP_016865462.1:p.Val1320Leu
XM_017009974.2:c.*62G>C	XP_016865463.1:n.*62G>C
NR_003149.2:n.10856G>C