Canonical Allele Identifier: CA360396115

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008105T>C (hg19) ; chr5:g.90712288T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712288T>C , CM000667.2:g.90712288T>C	GRCh38
NC_000005.9:g.90008105T>C , CM000667.1:g.90008105T>C	GRCh37
NC_000005.8:g.90043861T>C	NCBI36
NG_007083.1:g.158489T>C
NG_007083.2:g.187945T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9044T>C MANE Select	ENSP00000384582.2:p.Ile3015Thr
ENST00000639431.1:c.265+36079T>C	ENSP00000491057.1:n.265+36079T>C
ENST00000639473.1:n.4503T>C
ENST00000640012.1:c.2851T>C
ENST00000640374.1:n.2188T>C
ENST00000640779.1:c.3773T>C
ENST00000405460.6:c.9044T>C	ENSP00000384582.2:p.Ile3015Thr
ENST00000509621.1:c.1741T>C
NM_032119.3:c.9044T>C	NP_115495.3:p.Ile3015Thr
NR_003149.1:n.9057T>C
XM_011543675.1:c.9041T>C	XP_011541977.1:p.Ile3014Thr
XM_011543676.1:c.8963T>C	XP_011541978.1:p.Ile2988Thr
XM_011543677.1:c.6347T>C	XP_011541979.1:p.Ile2116Thr
XM_011543678.1:c.9044T>C	XP_011541980.1:p.Ile3015Thr
XM_011543679.1:c.9044T>C	XP_011541981.1:p.Ile3015Thr
NM_032119.4:c.9044T>C MANE Select	NP_115495.3:p.Ile3015Thr
XM_017009963.2:c.9065T>C	XP_016865452.1:p.Ile3022Thr
XM_017009964.2:c.9062T>C	XP_016865453.1:p.Ile3021Thr
XM_017009965.1:c.9062T>C	XP_016865454.1:p.Ile3021Thr
XM_017009966.2:c.8984T>C	XP_016865455.1:p.Ile2995Thr
XM_017009967.1:c.8969T>C	XP_016865456.1:p.Ile2990Thr
XM_017009968.2:c.9065T>C	XP_016865457.1:p.Ile3022Thr
XM_017009969.2:c.9065T>C	XP_016865458.1:p.Ile3022Thr
XM_017009970.2:c.9065T>C	XP_016865459.1:p.Ile3022Thr
XM_017009971.2:c.9065T>C	XP_016865460.1:p.Ile3022Thr
XM_017009972.1:c.2183T>C	XP_016865461.1:p.Ile728Thr
XM_017009973.1:c.2162T>C	XP_016865462.1:p.Ile721Thr
XM_017009974.2:c.9065T>C	XP_016865463.1:p.Ile3022Thr
NR_003149.2:n.9060T>C