Canonical Allele Identifier: CA3340347

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90708854T>C , CM000667.2:g.90708854T>C	GRCh38
NC_000005.9:g.90004671T>C , CM000667.1:g.90004671T>C	GRCh37
NC_000005.8:g.90040427T>C	NCBI36
NG_007083.1:g.155055T>C
NG_007083.2:g.184511T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.8769T>C MANE Select	NP_115495.3:p.Asn2923=
ENST00000405460.9:c.8769T>C MANE Select	ENSP00000384582.2:p.Asn2923=
NM_032119.3:c.8769T>C	NP_115495.3:p.Asn2923=
NR_003149.1:n.8782T>C
NR_003149.2:n.8785T>C
ENST00000405460.6:c.8769T>C	ENSP00000384582.2:p.Asn2923=
ENST00000509621.1:c.1466T>C
ENST00000639431.1:c.265+32645T>C	ENSP00000491057.1:n.265+32645T>C
ENST00000639473.1:n.4228T>C
ENST00000640012.1:c.2576T>C
ENST00000640374.1:n.1913T>C
ENST00000640403.1:c.6060T>C	ENSP00000492531.1:p.Asn2020=
ENST00000640779.1:c.3498T>C
XM_011543675.1:c.8766T>C	XP_011541977.1:p.Asn2922=
XM_011543676.1:c.8688T>C	XP_011541978.1:p.Asn2896=
XM_011543677.1:c.6072T>C	XP_011541979.1:p.Asn2024=
XM_011543678.1:c.8769T>C	XP_011541980.1:p.Asn2923=
XM_011543679.1:c.8769T>C	XP_011541981.1:p.Asn2923=
XM_017009963.2:c.8790T>C	XP_016865452.1:p.Asn2930=
XM_017009964.2:c.8787T>C	XP_016865453.1:p.Asn2929=
XM_017009965.1:c.8787T>C	XP_016865454.1:p.Asn2929=
XM_017009966.2:c.8709T>C	XP_016865455.1:p.Asn2903=
XM_017009967.1:c.8694T>C	XP_016865456.1:p.Asn2898=
XM_017009968.2:c.8790T>C	XP_016865457.1:p.Asn2930=
XM_017009969.2:c.8790T>C	XP_016865458.1:p.Asn2930=
XM_017009970.2:c.8790T>C	XP_016865459.1:p.Asn2930=
XM_017009971.2:c.8790T>C	XP_016865460.1:p.Asn2930=
XM_017009972.1:c.1908T>C	XP_016865461.1:p.Asn636=
XM_017009973.1:c.1887T>C	XP_016865462.1:p.Asn629=
XM_017009974.2:c.8790T>C	XP_016865463.1:p.Asn2930=