Canonical Allele Identifier: CA360403228

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725579C>T , CM000667.2:g.90725579C>T	GRCh38
NC_000005.9:g.90021396C>T , CM000667.1:g.90021396C>T	GRCh37
NC_000005.8:g.90057152C>T	NCBI36
NG_007083.1:g.171780C>T
NG_007083.2:g.201236C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.10084C>T MANE Select	NP_115495.3:p.Gln3362Ter
ENST00000405460.9:c.10084C>T MANE Select	ENSP00000384582.2:p.Gln3362Ter
NM_032119.3:c.10084C>T	NP_115495.3:p.Gln3362Ter
NR_003149.1:n.10097C>T
NR_003149.2:n.10100C>T
ENST00000405460.6:c.10084C>T	ENSP00000384582.2:p.Gln3362Ter
ENST00000509621.1:c.2781C>T
ENST00000639431.1:c.265+49370C>T	ENSP00000491057.1:n.265+49370C>T
ENST00000640374.1:n.3228C>T
ENST00000640464.1:n.503C>T
XM_011543675.1:c.10081C>T	XP_011541977.1:p.Gln3361Ter
XM_011543676.1:c.10003C>T	XP_011541978.1:p.Gln3335Ter
XM_011543677.1:c.7387C>T	XP_011541979.1:p.Gln2463Ter
XM_011543678.1:c.10084C>T	XP_011541980.1:p.Gln3362Ter
XM_011543679.1:c.10084C>T	XP_011541981.1:p.Gln3362Ter
XM_017009963.2:c.10105C>T	XP_016865452.1:p.Gln3369Ter
XM_017009964.2:c.10102C>T	XP_016865453.1:p.Gln3368Ter
XM_017009965.1:c.10102C>T	XP_016865454.1:p.Gln3368Ter
XM_017009966.2:c.10024C>T	XP_016865455.1:p.Gln3342Ter
XM_017009967.1:c.10009C>T	XP_016865456.1:p.Gln3337Ter
XM_017009968.2:c.10105C>T	XP_016865457.1:p.Gln3369Ter
XM_017009969.2:c.10105C>T	XP_016865458.1:p.Gln3369Ter
XM_017009970.2:c.10105C>T	XP_016865459.1:p.Gln3369Ter
XM_017009971.2:c.10105C>T	XP_016865460.1:p.Gln3369Ter
XM_017009972.1:c.3223C>T	XP_016865461.1:p.Gln1075Ter
XM_017009973.1:c.3202C>T	XP_016865462.1:p.Gln1068Ter
XM_017009974.2:c.10105C>T	XP_016865463.1:p.Gln3369Ter
XR_001742802.1:n.2523-9770G>A
XR_948560.1:n.272-9770G>A