Canonical Allele Identifier: CA3340517

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720076C>T , CM000667.2:g.90720076C>T	GRCh38
NC_000005.9:g.90015893C>T , CM000667.1:g.90015893C>T	GRCh37
NC_000005.8:g.90051649C>T	NCBI36
NG_007083.1:g.166277C>T
NG_007083.2:g.195733C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9476C>T MANE Select	NP_115495.3:p.Thr3159Met
ENST00000405460.9:c.9476C>T MANE Select	ENSP00000384582.2:p.Thr3159Met
NM_032119.3:c.9476C>T	NP_115495.3:p.Thr3159Met
NR_003149.1:n.9489C>T
NR_003149.2:n.9492C>T
ENST00000405460.6:c.9476C>T	ENSP00000384582.2:p.Thr3159Met
ENST00000509621.1:c.2173C>T
ENST00000639431.1:c.265+43867C>T	ENSP00000491057.1:n.265+43867C>T
ENST00000640374.1:n.2620C>T
ENST00000640779.1:c.4205C>T
XM_011543675.1:c.9473C>T	XP_011541977.1:p.Thr3158Met
XM_011543676.1:c.9395C>T	XP_011541978.1:p.Thr3132Met
XM_011543677.1:c.6779C>T	XP_011541979.1:p.Thr2260Met
XM_011543678.1:c.9476C>T	XP_011541980.1:p.Thr3159Met
XM_011543679.1:c.9476C>T	XP_011541981.1:p.Thr3159Met
XM_017009963.2:c.9497C>T	XP_016865452.1:p.Thr3166Met
XM_017009964.2:c.9494C>T	XP_016865453.1:p.Thr3165Met
XM_017009965.1:c.9494C>T	XP_016865454.1:p.Thr3165Met
XM_017009966.2:c.9416C>T	XP_016865455.1:p.Thr3139Met
XM_017009967.1:c.9401C>T	XP_016865456.1:p.Thr3134Met
XM_017009968.2:c.9497C>T	XP_016865457.1:p.Thr3166Met
XM_017009969.2:c.9497C>T	XP_016865458.1:p.Thr3166Met
XM_017009970.2:c.9497C>T	XP_016865459.1:p.Thr3166Met
XM_017009971.2:c.9497C>T	XP_016865460.1:p.Thr3166Met
XM_017009972.1:c.2615C>T	XP_016865461.1:p.Thr872Met
XM_017009973.1:c.2594C>T	XP_016865462.1:p.Thr865Met
XM_017009974.2:c.9497C>T	XP_016865463.1:p.Thr3166Met
XR_001742802.1:n.2523-4267G>A
XR_948560.1:n.272-4267G>A