Canonical Allele Identifier: CA3340241

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90704500T>C , CM000667.2:g.90704500T>C	GRCh38
NC_000005.9:g.90000317T>C , CM000667.1:g.90000317T>C	GRCh37
NC_000005.8:g.90036073T>C	NCBI36
NG_007083.1:g.150701T>C
NG_007083.2:g.180157T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.8386+12T>C MANE Select	NP_115495.3:n.8386+12T>C
ENST00000405460.9:c.8386+12T>C MANE Select	ENSP00000384582.2:n.8386+12T>C
NM_032119.3:c.8386+12T>C	NP_115495.3:n.8386+12T>C
NR_003149.1:n.8399+12T>C
NR_003149.2:n.8402+12T>C
ENST00000405460.6:c.8386+12T>C	ENSP00000384582.2:n.8386+12T>C
ENST00000509621.1:c.1083+12T>C
ENST00000639431.1:c.265+28291T>C	ENSP00000491057.1:n.265+28291T>C
ENST00000639473.1:n.3845+12T>C
ENST00000640012.1:c.2193+12T>C
ENST00000640374.1:n.1530+12T>C
ENST00000640403.1:c.5677+12T>C	ENSP00000492531.1:n.5677+12T>C
ENST00000640779.1:c.3115+12T>C
XM_011543675.1:c.8383+12T>C	XP_011541977.1:n.8383+12T>C
XM_011543676.1:c.8305+12T>C	XP_011541978.1:n.8305+12T>C
XM_011543677.1:c.5689+12T>C	XP_011541979.1:n.5689+12T>C
XM_011543678.1:c.8386+12T>C	XP_011541980.1:n.8386+12T>C
XM_011543679.1:c.8386+12T>C	XP_011541981.1:n.8386+12T>C
XM_017009963.2:c.8386+12T>C	XP_016865452.1:n.8386+12T>C
XM_017009964.2:c.8383+12T>C	XP_016865453.1:n.8383+12T>C
XM_017009965.1:c.8383+12T>C	XP_016865454.1:n.8383+12T>C
XM_017009966.2:c.8305+12T>C	XP_016865455.1:n.8305+12T>C
XM_017009967.1:c.8290+12T>C	XP_016865456.1:n.8290+12T>C
XM_017009968.2:c.8386+12T>C	XP_016865457.1:n.8386+12T>C
XM_017009969.2:c.8386+12T>C	XP_016865458.1:n.8386+12T>C
XM_017009970.2:c.8386+12T>C	XP_016865459.1:n.8386+12T>C
XM_017009971.2:c.8386+12T>C	XP_016865460.1:n.8386+12T>C
XM_017009972.1:c.1504+12T>C	XP_016865461.1:n.1504+12T>C
XM_017009973.1:c.1504+12T>C	XP_016865462.1:n.1504+12T>C
XM_017009974.2:c.8386+12T>C	XP_016865463.1:n.8386+12T>C