Canonical Allele Identifier: CA360429033

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90985343G>C , CM000667.2:g.90985343G>C	GRCh38
NC_000005.9:g.90281160G>C , CM000667.1:g.90281160G>C	GRCh37
NC_000005.8:g.90316916G>C	NCBI36
NG_007083.1:g.431544G>C
NG_007083.2:g.461000G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17974-1G>C MANE Select	NP_115495.3:n.17974-1G>C
ENST00000405460.9:c.17974-1G>C MANE Select	ENSP00000384582.2:n.17974-1G>C
NM_032119.3:c.17974-1G>C	NP_115495.3:n.17974-1G>C
NR_003149.1:n.17987-1G>C
NR_003149.2:n.17990-1G>C
ENST00000405460.6:c.17974-1G>C	ENSP00000384582.2:n.17974-1G>C
ENST00000425867.2:c.4957-1G>C	ENSP00000392618.2:n.4957-1G>C
ENST00000425867.3:c.6928-1G>C	ENSP00000392618.3:n.6928-1G>C
ENST00000638510.1:n.5241-1G>C
ENST00000638990.1:c.1186-1G>C
ENST00000639431.1:c.266-1G>C	ENSP00000491057.1:n.266-1G>C
ENST00000639707.1:c.58-1G>C	ENSP00000492328.1:n.58-1G>C
ENST00000639821.1:c.58-1G>C	ENSP00000492216.1:n.58-1G>C
ENST00000640369.1:c.58-1G>C	ENSP00000491401.1:n.58-1G>C
ENST00000640407.1:c.4423-1G>C	ENSP00000491425.1:n.4423-1G>C
ENST00000640815.1:c.58-1G>C	ENSP00000491767.1:n.58-1G>C
XM_011543675.1:c.17971-1G>C	XP_011541977.1:n.17971-1G>C
XM_011543676.1:c.17893-1G>C	XP_011541978.1:n.17893-1G>C
XM_011543677.1:c.15277-1G>C	XP_011541979.1:n.15277-1G>C
XM_017009963.2:c.17995-1G>C	XP_016865452.1:n.17995-1G>C
XM_017009964.2:c.17992-1G>C	XP_016865453.1:n.17992-1G>C
XM_017009965.1:c.17992-1G>C	XP_016865454.1:n.17992-1G>C
XM_017009966.2:c.17914-1G>C	XP_016865455.1:n.17914-1G>C
XM_017009967.1:c.17899-1G>C	XP_016865456.1:n.17899-1G>C
XM_017009968.2:c.17815-1G>C	XP_016865457.1:n.17815-1G>C
XM_017009969.2:c.17995-1G>C	XP_016865458.1:n.17995-1G>C
XM_017009972.1:c.11113-1G>C	XP_016865461.1:n.11113-1G>C
XM_017009973.1:c.11092-1G>C	XP_016865462.1:n.11092-1G>C