Canonical Allele Identifier: CA3338688

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90628800C>T , CM000667.2:g.90628800C>T	GRCh38
NC_000005.9:g.89924617C>T , CM000667.1:g.89924617C>T	GRCh37
NC_000005.8:g.89960373C>T	NCBI36
NG_007083.1:g.75001C>T
NG_007083.2:g.104457C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.1477C>T MANE Select	NP_115495.3:p.Arg493Ter
ENST00000405460.9:c.1477C>T MANE Select	ENSP00000384582.2:p.Arg493Ter
NM_032119.3:c.1477C>T	NP_115495.3:p.Arg493Ter
NR_003149.1:n.1573C>T
NR_003149.2:n.1576C>T
ENST00000405460.6:c.1477C>T	ENSP00000384582.2:p.Arg493Ter
ENST00000504142.1:c.242C>T
ENST00000504142.2:n.243C>T
ENST00000640083.1:n.1182C>T
ENST00000640109.1:n.1573C>T
XM_011543675.1:c.1477C>T	XP_011541977.1:p.Arg493Ter
XM_011543676.1:c.1477C>T	XP_011541978.1:p.Arg493Ter
XM_011543678.1:c.1477C>T	XP_011541980.1:p.Arg493Ter
XM_011543679.1:c.1477C>T	XP_011541981.1:p.Arg493Ter
XM_017009963.2:c.1477C>T	XP_016865452.1:p.Arg493Ter
XM_017009964.2:c.1477C>T	XP_016865453.1:p.Arg493Ter
XM_017009965.1:c.1474C>T	XP_016865454.1:p.Arg492Ter
XM_017009966.2:c.1477C>T	XP_016865455.1:p.Arg493Ter
XM_017009967.1:c.1381C>T	XP_016865456.1:p.Arg461Ter
XM_017009968.2:c.1477C>T	XP_016865457.1:p.Arg493Ter
XM_017009969.2:c.1477C>T	XP_016865458.1:p.Arg493Ter
XM_017009970.2:c.1477C>T	XP_016865459.1:p.Arg493Ter
XM_017009971.2:c.1477C>T	XP_016865460.1:p.Arg493Ter
XM_017009974.2:c.1477C>T	XP_016865463.1:p.Arg493Ter