Canonical Allele Identifier: CA360383831

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90774261C>T , CM000667.2:g.90774261C>T	GRCh38
NC_000005.9:g.90070078C>T , CM000667.1:g.90070078C>T	GRCh37
NC_000005.8:g.90105834C>T	NCBI36
NG_007083.1:g.220462C>T
NG_007083.2:g.249918C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12361C>T MANE Select	NP_115495.3:p.Gln4121Ter
ENST00000405460.9:c.12361C>T MANE Select	ENSP00000384582.2:p.Gln4121Ter
NM_032119.3:c.12361C>T	NP_115495.3:p.Gln4121Ter
NR_003149.1:n.12374C>T
NR_003149.2:n.12377C>T
ENST00000405460.6:c.12361C>T	ENSP00000384582.2:p.Gln4121Ter
ENST00000425867.3:c.1315C>T	ENSP00000392618.3:p.Gln439Ter
ENST00000639431.1:c.265+98052C>T	ENSP00000491057.1:n.265+98052C>T
ENST00000640464.1:n.2780C>T
ENST00000640729.1:n.938C>T
XM_011543675.1:c.12358C>T	XP_011541977.1:p.Gln4120Ter
XM_011543676.1:c.12280C>T	XP_011541978.1:p.Gln4094Ter
XM_011543677.1:c.9664C>T	XP_011541979.1:p.Gln3222Ter
XM_011543678.1:c.12361C>T	XP_011541980.1:p.Gln4121Ter
XM_017009963.2:c.12382C>T	XP_016865452.1:p.Gln4128Ter
XM_017009964.2:c.12379C>T	XP_016865453.1:p.Gln4127Ter
XM_017009965.1:c.12379C>T	XP_016865454.1:p.Gln4127Ter
XM_017009966.2:c.12301C>T	XP_016865455.1:p.Gln4101Ter
XM_017009967.1:c.12286C>T	XP_016865456.1:p.Gln4096Ter
XM_017009968.2:c.12382C>T	XP_016865457.1:p.Gln4128Ter
XM_017009969.2:c.12382C>T	XP_016865458.1:p.Gln4128Ter
XM_017009970.2:c.12382C>T	XP_016865459.1:p.Gln4128Ter
XM_017009971.2:c.12382C>T	XP_016865460.1:p.Gln4128Ter
XM_017009972.1:c.5500C>T	XP_016865461.1:p.Gln1834Ter
XM_017009973.1:c.5479C>T	XP_016865462.1:p.Gln1827Ter