Canonical Allele Identifier: CA360398378

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789705C>T , CM000667.2:g.90789705C>T	GRCh38
NC_000005.9:g.90085522C>T , CM000667.1:g.90085522C>T	GRCh37
NC_000005.8:g.90121278C>T	NCBI36
NG_007083.1:g.235906C>T
NG_007083.2:g.265362C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13897C>T MANE Select	NP_115495.3:p.Gln4633Ter
ENST00000405460.9:c.13897C>T MANE Select	ENSP00000384582.2:p.Gln4633Ter
NM_032119.3:c.13897C>T	NP_115495.3:p.Gln4633Ter
NR_003149.1:n.13910C>T
NR_003149.2:n.13913C>T
ENST00000405460.6:c.13897C>T	ENSP00000384582.2:p.Gln4633Ter
ENST00000425867.2:c.880C>T	ENSP00000392618.2:p.Gln294Ter
ENST00000425867.3:c.2851C>T	ENSP00000392618.3:p.Gln951Ter
ENST00000638510.1:n.1164C>T
ENST00000638975.1:c.526C>T	ENSP00000492630.1:p.Gln176Ter
ENST00000639431.1:c.265+113496C>T	ENSP00000491057.1:n.265+113496C>T
ENST00000640407.1:c.307C>T	ENSP00000491425.1:p.Gln103Ter
XM_011543675.1:c.13894C>T	XP_011541977.1:p.Gln4632Ter
XM_011543676.1:c.13816C>T	XP_011541978.1:p.Gln4606Ter
XM_011543677.1:c.11200C>T	XP_011541979.1:p.Gln3734Ter
XM_011543678.1:c.13897C>T	XP_011541980.1:p.Gln4633Ter
XM_017009963.2:c.13918C>T	XP_016865452.1:p.Gln4640Ter
XM_017009964.2:c.13915C>T	XP_016865453.1:p.Gln4639Ter
XM_017009965.1:c.13915C>T	XP_016865454.1:p.Gln4639Ter
XM_017009966.2:c.13837C>T	XP_016865455.1:p.Gln4613Ter
XM_017009967.1:c.13822C>T	XP_016865456.1:p.Gln4608Ter
XM_017009968.2:c.13918C>T	XP_016865457.1:p.Gln4640Ter
XM_017009969.2:c.13918C>T	XP_016865458.1:p.Gln4640Ter
XM_017009970.2:c.13918C>T	XP_016865459.1:p.Gln4640Ter
XM_017009971.2:c.13918C>T	XP_016865460.1:p.Gln4640Ter
XM_017009972.1:c.7036C>T	XP_016865461.1:p.Gln2346Ter
XM_017009973.1:c.7015C>T	XP_016865462.1:p.Gln2339Ter