Canonical Allele Identifier: CA2767405910

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716757G>C , CM000667.2:g.90716757G>C	GRCh38
NC_000005.9:g.90012574G>C , CM000667.1:g.90012574G>C	GRCh37
NC_000005.8:g.90048330G>C	NCBI36
NG_007083.1:g.162958G>C
NG_007083.2:g.192414G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9447+28G>C MANE Select	ENSP00000384582.2:n.9447+28G>C
ENST00000639431.1:c.265+40548G>C	ENSP00000491057.1:n.265+40548G>C
ENST00000639473.1:n.4934G>C
ENST00000640374.1:n.2591+28G>C
ENST00000640779.1:c.4176+28G>C
ENST00000405460.6:c.9447+28G>C	ENSP00000384582.2:n.9447+28G>C
ENST00000509621.1:c.2144+28G>C
NM_032119.3:c.9447+28G>C	NP_115495.3:n.9447+28G>C
NR_003149.1:n.9460+28G>C
XM_011543675.1:c.9444+28G>C	XP_011541977.1:n.9444+28G>C
XM_011543676.1:c.9366+28G>C	XP_011541978.1:n.9366+28G>C
XM_011543677.1:c.6750+28G>C	XP_011541979.1:n.6750+28G>C
XM_011543678.1:c.9447+28G>C	XP_011541980.1:n.9447+28G>C
XM_011543679.1:c.9447+28G>C	XP_011541981.1:n.9447+28G>C
XR_948560.1:n.272-948C>G
NM_032119.4:c.9447+28G>C MANE Select	NP_115495.3:n.9447+28G>C
XM_017009963.2:c.9468+28G>C	XP_016865452.1:n.9468+28G>C
XM_017009964.2:c.9465+28G>C	XP_016865453.1:n.9465+28G>C
XM_017009965.1:c.9465+28G>C	XP_016865454.1:n.9465+28G>C
XM_017009966.2:c.9387+28G>C	XP_016865455.1:n.9387+28G>C
XM_017009967.1:c.9372+28G>C	XP_016865456.1:n.9372+28G>C
XM_017009968.2:c.9468+28G>C	XP_016865457.1:n.9468+28G>C
XM_017009969.2:c.9468+28G>C	XP_016865458.1:n.9468+28G>C
XM_017009970.2:c.9468+28G>C	XP_016865459.1:n.9468+28G>C
XM_017009971.2:c.9468+28G>C	XP_016865460.1:n.9468+28G>C
XM_017009972.1:c.2586+28G>C	XP_016865461.1:n.2586+28G>C
XM_017009973.1:c.2565+28G>C	XP_016865462.1:n.2565+28G>C
XM_017009974.2:c.9468+28G>C	XP_016865463.1:n.9468+28G>C
XR_001742802.1:n.2523-948C>G
NR_003149.2:n.9463+28G>C