Canonical Allele Identifier: CA360406059

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90805282A>C , CM000667.2:g.90805282A>C	GRCh38
NC_000005.9:g.90101099A>C , CM000667.1:g.90101099A>C	GRCh37
NC_000005.8:g.90136855A>C	NCBI36
NG_007083.1:g.251483A>C
NG_007083.2:g.280939A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14662-2A>C MANE Select	NP_115495.3:n.14662-2A>C
ENST00000405460.9:c.14662-2A>C MANE Select	ENSP00000384582.2:n.14662-2A>C
NM_032119.3:c.14662-2A>C	NP_115495.3:n.14662-2A>C
NR_003149.1:n.14675-2A>C
NR_003149.2:n.14678-2A>C
ENST00000405460.6:c.14662-2A>C	ENSP00000384582.2:n.14662-2A>C
ENST00000425867.2:c.1645-2A>C	ENSP00000392618.2:n.1645-2A>C
ENST00000425867.3:c.3616-2A>C	ENSP00000392618.3:n.3616-2A>C
ENST00000513828.1:n.356A>C
ENST00000638510.1:n.1929-2A>C
ENST00000638585.1:n.427+2400A>C
ENST00000639431.1:c.265+129073A>C	ENSP00000491057.1:n.265+129073A>C
ENST00000640407.1:c.1072-2A>C	ENSP00000491425.1:n.1072-2A>C
XM_011543675.1:c.14659-2A>C	XP_011541977.1:n.14659-2A>C
XM_011543676.1:c.14581-2A>C	XP_011541978.1:n.14581-2A>C
XM_011543677.1:c.11965-2A>C	XP_011541979.1:n.11965-2A>C
XM_011543678.1:c.14662-2A>C	XP_011541980.1:n.14662-2A>C
XM_017009963.2:c.14683-2A>C	XP_016865452.1:n.14683-2A>C
XM_017009964.2:c.14680-2A>C	XP_016865453.1:n.14680-2A>C
XM_017009965.1:c.14680-2A>C	XP_016865454.1:n.14680-2A>C
XM_017009966.2:c.14602-2A>C	XP_016865455.1:n.14602-2A>C
XM_017009967.1:c.14587-2A>C	XP_016865456.1:n.14587-2A>C
XM_017009968.2:c.14683-2320A>C	XP_016865457.1:n.14683-2320A>C
XM_017009969.2:c.14683-2A>C	XP_016865458.1:n.14683-2A>C
XM_017009970.2:c.14683-2A>C	XP_016865459.1:n.14683-2A>C
XM_017009971.2:c.14683-2320A>C	XP_016865460.1:n.14683-2320A>C
XM_017009972.1:c.7801-2A>C	XP_016865461.1:n.7801-2A>C
XM_017009973.1:c.7780-2A>C	XP_016865462.1:n.7780-2A>C