Canonical Allele Identifier: CA3339356

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90657998C>T , CM000667.2:g.90657998C>T	GRCh38
NC_000005.9:g.89953815C>T , CM000667.1:g.89953815C>T	GRCh37
NC_000005.8:g.89989571C>T	NCBI36
NG_007083.1:g.104199C>T
NG_007083.2:g.133655C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.4472C>T MANE Select	NP_115495.3:p.Thr1491Met
ENST00000405460.9:c.4472C>T MANE Select	ENSP00000384582.2:p.Thr1491Met
NM_032119.3:c.4472C>T	NP_115495.3:p.Thr1491Met
NR_003149.1:n.4568C>T
NR_003149.2:n.4571C>T
ENST00000405460.6:c.4472C>T	ENSP00000384582.2:p.Thr1491Met
ENST00000639676.1:n.2070C>T
ENST00000640403.1:c.1763C>T	ENSP00000492531.1:p.Thr588Met
XM_011543675.1:c.4472C>T	XP_011541977.1:p.Thr1491Met
XM_011543676.1:c.4472C>T	XP_011541978.1:p.Thr1491Met
XM_011543677.1:c.1775C>T	XP_011541979.1:p.Thr592Met
XM_011543678.1:c.4472C>T	XP_011541980.1:p.Thr1491Met
XM_011543679.1:c.4472C>T	XP_011541981.1:p.Thr1491Met
XM_017009963.2:c.4472C>T	XP_016865452.1:p.Thr1491Met
XM_017009964.2:c.4472C>T	XP_016865453.1:p.Thr1491Met
XM_017009965.1:c.4469C>T	XP_016865454.1:p.Thr1490Met
XM_017009966.2:c.4472C>T	XP_016865455.1:p.Thr1491Met
XM_017009967.1:c.4376C>T	XP_016865456.1:p.Thr1459Met
XM_017009968.2:c.4472C>T	XP_016865457.1:p.Thr1491Met
XM_017009969.2:c.4472C>T	XP_016865458.1:p.Thr1491Met
XM_017009970.2:c.4472C>T	XP_016865459.1:p.Thr1491Met
XM_017009971.2:c.4472C>T	XP_016865460.1:p.Thr1491Met
XM_017009974.2:c.4472C>T	XP_016865463.1:p.Thr1491Met