Canonical Allele Identifier: CA3339426

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90672664T>C , CM000667.2:g.90672664T>C	GRCh38
NC_000005.9:g.89968481T>C , CM000667.1:g.89968481T>C	GRCh37
NC_000005.8:g.90004237T>C	NCBI36
NG_007083.1:g.118865T>C
NG_007083.2:g.148321T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.4871T>C MANE Select	NP_115495.3:p.Val1624Ala
ENST00000405460.9:c.4871T>C MANE Select	ENSP00000384582.2:p.Val1624Ala
NM_032119.3:c.4871T>C	NP_115495.3:p.Val1624Ala
NR_003149.1:n.4967T>C
NR_003149.2:n.4970T>C
ENST00000405460.6:c.4871T>C	ENSP00000384582.2:p.Val1624Ala
ENST00000450321.2:n.111T>C
ENST00000639473.1:n.330T>C
ENST00000639676.1:n.2469T>C
ENST00000640403.1:c.2162T>C	ENSP00000492531.1:p.Val721Ala
XM_011543675.1:c.4871T>C	XP_011541977.1:p.Val1624Ala
XM_011543676.1:c.4871T>C	XP_011541978.1:p.Val1624Ala
XM_011543677.1:c.2174T>C	XP_011541979.1:p.Val725Ala
XM_011543678.1:c.4871T>C	XP_011541980.1:p.Val1624Ala
XM_011543679.1:c.4871T>C	XP_011541981.1:p.Val1624Ala
XM_017009963.2:c.4871T>C	XP_016865452.1:p.Val1624Ala
XM_017009964.2:c.4871T>C	XP_016865453.1:p.Val1624Ala
XM_017009965.1:c.4868T>C	XP_016865454.1:p.Val1623Ala
XM_017009966.2:c.4871T>C	XP_016865455.1:p.Val1624Ala
XM_017009967.1:c.4775T>C	XP_016865456.1:p.Val1592Ala
XM_017009968.2:c.4871T>C	XP_016865457.1:p.Val1624Ala
XM_017009969.2:c.4871T>C	XP_016865458.1:p.Val1624Ala
XM_017009970.2:c.4871T>C	XP_016865459.1:p.Val1624Ala
XM_017009971.2:c.4871T>C	XP_016865460.1:p.Val1624Ala
XM_017009974.2:c.4871T>C	XP_016865463.1:p.Val1624Ala