Canonical Allele Identifier: CA3342001

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811159C>G , CM000667.2:g.90811159C>G	GRCh38
NC_000005.9:g.90106976C>G , CM000667.1:g.90106976C>G	GRCh37
NC_000005.8:g.90142732C>G	NCBI36
NG_007083.1:g.257360C>G
NG_007083.2:g.286816C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15899C>G MANE Select	NP_115495.3:p.Thr5300Ser
ENST00000405460.9:c.15899C>G MANE Select	ENSP00000384582.2:p.Thr5300Ser
NM_032119.3:c.15899C>G	NP_115495.3:p.Thr5300Ser
NR_003149.1:n.15912C>G
NR_003149.2:n.15915C>G
ENST00000405460.6:c.15899C>G	ENSP00000384582.2:p.Thr5300Ser
ENST00000425867.2:c.2882C>G	ENSP00000392618.2:p.Thr961Ser
ENST00000425867.3:c.4853C>G	ENSP00000392618.3:p.Thr1618Ser
ENST00000638510.1:n.3166C>G
ENST00000639431.1:c.265+134950C>G	ENSP00000491057.1:n.265+134950C>G
ENST00000640407.1:c.2309C>G	ENSP00000491425.1:p.Thr770Ser
XM_011543675.1:c.15896C>G	XP_011541977.1:p.Thr5299Ser
XM_011543676.1:c.15818C>G	XP_011541978.1:p.Thr5273Ser
XM_011543677.1:c.13202C>G	XP_011541979.1:p.Thr4401Ser
XM_017009963.2:c.15920C>G	XP_016865452.1:p.Thr5307Ser
XM_017009964.2:c.15917C>G	XP_016865453.1:p.Thr5306Ser
XM_017009965.1:c.15917C>G	XP_016865454.1:p.Thr5306Ser
XM_017009966.2:c.15839C>G	XP_016865455.1:p.Thr5280Ser
XM_017009967.1:c.15824C>G	XP_016865456.1:p.Thr5275Ser
XM_017009968.2:c.15740C>G	XP_016865457.1:p.Thr5247Ser
XM_017009969.2:c.15920C>G	XP_016865458.1:p.Thr5307Ser
XM_017009972.1:c.9038C>G	XP_016865461.1:p.Thr3013Ser
XM_017009973.1:c.9017C>G	XP_016865462.1:p.Thr3006Ser