Canonical Allele Identifier: CA208796

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745193T>C , CM000667.2:g.90745193T>C	GRCh38
NC_000005.9:g.90041010T>C , CM000667.1:g.90041010T>C	GRCh37
NC_000005.8:g.90076766T>C	NCBI36
NG_007083.1:g.191394T>C
NG_007083.2:g.220850T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.10697T>C MANE Select	NP_115495.3:p.Ile3566Thr
ENST00000405460.9:c.10697T>C MANE Select	ENSP00000384582.2:p.Ile3566Thr
NM_032119.3:c.10697T>C	NP_115495.3:p.Ile3566Thr
NR_003149.1:n.10710T>C
NR_003149.2:n.10713T>C
ENST00000405460.6:c.10697T>C	ENSP00000384582.2:p.Ile3566Thr
ENST00000509621.1:c.3394T>C
ENST00000639431.1:c.265+68984T>C	ENSP00000491057.1:n.265+68984T>C
ENST00000640374.1:n.3841T>C
ENST00000640464.1:n.1116T>C
XM_011543675.1:c.10694T>C	XP_011541977.1:p.Ile3565Thr
XM_011543676.1:c.10616T>C	XP_011541978.1:p.Ile3539Thr
XM_011543677.1:c.8000T>C	XP_011541979.1:p.Ile2667Thr
XM_011543678.1:c.10697T>C	XP_011541980.1:p.Ile3566Thr
XM_011543679.1:c.10697T>C	XP_011541981.1:p.Ile3566Thr
XM_017009963.2:c.10718T>C	XP_016865452.1:p.Ile3573Thr
XM_017009964.2:c.10715T>C	XP_016865453.1:p.Ile3572Thr
XM_017009965.1:c.10715T>C	XP_016865454.1:p.Ile3572Thr
XM_017009966.2:c.10637T>C	XP_016865455.1:p.Ile3546Thr
XM_017009967.1:c.10622T>C	XP_016865456.1:p.Ile3541Thr
XM_017009968.2:c.10718T>C	XP_016865457.1:p.Ile3573Thr
XM_017009969.2:c.10718T>C	XP_016865458.1:p.Ile3573Thr
XM_017009970.2:c.10718T>C	XP_016865459.1:p.Ile3573Thr
XM_017009971.2:c.10718T>C	XP_016865460.1:p.Ile3573Thr
XM_017009972.1:c.3836T>C	XP_016865461.1:p.Ile1279Thr
XM_017009973.1:c.3815T>C	XP_016865462.1:p.Ile1272Thr
XM_017009974.2:c.10718T>C	XP_016865463.1:p.Ile3573Thr