Canonical Allele Identifier: CA3342457

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90863795A>C , CM000667.2:g.90863795A>C	GRCh38
NC_000005.9:g.90159612A>C , CM000667.1:g.90159612A>C	GRCh37
NC_000005.8:g.90195368A>C	NCBI36
NG_007083.1:g.309996A>C
NG_007083.2:g.339452A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17794A>C MANE Select	NP_115495.3:p.Arg5932=
ENST00000405460.9:c.17794A>C MANE Select	ENSP00000384582.2:p.Arg5932=
NM_032119.3:c.17794A>C	NP_115495.3:p.Arg5932=
NR_003149.1:n.17807A>C
NR_003149.2:n.17810A>C
ENST00000405460.6:c.17794A>C	ENSP00000384582.2:p.Arg5932=
ENST00000425867.2:c.4777A>C	ENSP00000392618.2:p.Arg1593=
ENST00000425867.3:c.6748A>C	ENSP00000392618.3:p.Arg2250=
ENST00000503852.1:n.342A>C
ENST00000638510.1:n.5061A>C
ENST00000638990.1:c.1006A>C
ENST00000639431.1:c.266-121549A>C	ENSP00000491057.1:n.266-121549A>C
ENST00000640407.1:c.4243A>C	ENSP00000491425.1:n.4243A>C
XM_011543675.1:c.17791A>C	XP_011541977.1:p.Arg5931=
XM_011543676.1:c.17713A>C	XP_011541978.1:p.Arg5905=
XM_011543677.1:c.15097A>C	XP_011541979.1:p.Arg5033=
XM_017009963.2:c.17815A>C	XP_016865452.1:p.Arg5939=
XM_017009964.2:c.17812A>C	XP_016865453.1:p.Arg5938=
XM_017009965.1:c.17812A>C	XP_016865454.1:p.Arg5938=
XM_017009966.2:c.17734A>C	XP_016865455.1:p.Arg5912=
XM_017009967.1:c.17719A>C	XP_016865456.1:p.Arg5907=
XM_017009968.2:c.17635A>C	XP_016865457.1:p.Arg5879=
XM_017009969.2:c.17815A>C	XP_016865458.1:p.Arg5939=
XM_017009972.1:c.10933A>C	XP_016865461.1:p.Arg3645=
XM_017009973.1:c.10912A>C	XP_016865462.1:p.Arg3638=