Canonical Allele Identifier: CA2767422801

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789930T>A , CM000667.2:g.90789930T>A	GRCh38
NC_000005.9:g.90085747T>A , CM000667.1:g.90085747T>A	GRCh37
NC_000005.8:g.90121503T>A	NCBI36
NG_007083.1:g.236131T>A
NG_007083.2:g.265587T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14043+79T>A MANE Select	ENSP00000384582.2:n.14043+79T>A
ENST00000425867.3:c.2997+79T>A	ENSP00000392618.3:n.2997+79T>A
ENST00000638510.1:n.1310+79T>A
ENST00000638975.1:c.672+79T>A	ENSP00000492630.1:n.672+79T>A
ENST00000639431.1:c.265+113721T>A	ENSP00000491057.1:n.265+113721T>A
ENST00000640407.1:c.453+79T>A	ENSP00000491425.1:n.453+79T>A
ENST00000405460.6:c.14043+79T>A	ENSP00000384582.2:n.14043+79T>A
ENST00000425867.2:c.1026+79T>A	ENSP00000392618.2:n.1026+79T>A
NM_032119.3:c.14043+79T>A	NP_115495.3:n.14043+79T>A
NR_003149.1:n.14056+79T>A
XM_011543675.1:c.14040+79T>A	XP_011541977.1:n.14040+79T>A
XM_011543676.1:c.13962+79T>A	XP_011541978.1:n.13962+79T>A
XM_011543677.1:c.11346+79T>A	XP_011541979.1:n.11346+79T>A
XM_011543678.1:c.14043+79T>A	XP_011541980.1:n.14043+79T>A
NM_032119.4:c.14043+79T>A MANE Select	NP_115495.3:n.14043+79T>A
XM_017009963.2:c.14064+79T>A	XP_016865452.1:n.14064+79T>A
XM_017009964.2:c.14061+79T>A	XP_016865453.1:n.14061+79T>A
XM_017009965.1:c.14061+79T>A	XP_016865454.1:n.14061+79T>A
XM_017009966.2:c.13983+79T>A	XP_016865455.1:n.13983+79T>A
XM_017009967.1:c.13968+79T>A	XP_016865456.1:n.13968+79T>A
XM_017009968.2:c.14064+79T>A	XP_016865457.1:n.14064+79T>A
XM_017009969.2:c.14064+79T>A	XP_016865458.1:n.14064+79T>A
XM_017009970.2:c.14064+79T>A	XP_016865459.1:n.14064+79T>A
XM_017009971.2:c.14064+79T>A	XP_016865460.1:n.14064+79T>A
XM_017009972.1:c.7182+79T>A	XP_016865461.1:n.7182+79T>A
XM_017009973.1:c.7161+79T>A	XP_016865462.1:n.7161+79T>A
NR_003149.2:n.14059+79T>A