Canonical Allele Identifier: CA360430245

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90853465C>T , CM000667.2:g.90853465C>T	GRCh38
NC_000005.9:g.90149282C>T , CM000667.1:g.90149282C>T	GRCh37
NC_000005.8:g.90185038C>T	NCBI36
NG_007083.1:g.299666C>T
NG_007083.2:g.329122C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17386C>T MANE Select	NP_115495.3:p.Gln5796Ter
ENST00000405460.9:c.17386C>T MANE Select	ENSP00000384582.2:p.Gln5796Ter
NM_032119.3:c.17386C>T	NP_115495.3:p.Gln5796Ter
NR_003149.1:n.17399C>T
NR_003149.2:n.17402C>T
ENST00000405460.6:c.17386C>T	ENSP00000384582.2:p.Gln5796Ter
ENST00000425867.2:c.4369C>T	ENSP00000392618.2:p.Gln1457Ter
ENST00000425867.3:c.6340C>T	ENSP00000392618.3:p.Gln2114Ter
ENST00000638510.1:n.4653C>T
ENST00000638990.1:c.598C>T
ENST00000639431.1:c.266-131879C>T	ENSP00000491057.1:n.266-131879C>T
ENST00000640407.1:c.3835C>T	ENSP00000491425.1:n.3835C>T
XM_011543675.1:c.17383C>T	XP_011541977.1:p.Gln5795Ter
XM_011543676.1:c.17305C>T	XP_011541978.1:p.Gln5769Ter
XM_011543677.1:c.14689C>T	XP_011541979.1:p.Gln4897Ter
XM_017009963.2:c.17407C>T	XP_016865452.1:p.Gln5803Ter
XM_017009964.2:c.17404C>T	XP_016865453.1:p.Gln5802Ter
XM_017009965.1:c.17404C>T	XP_016865454.1:p.Gln5802Ter
XM_017009966.2:c.17326C>T	XP_016865455.1:p.Gln5776Ter
XM_017009967.1:c.17311C>T	XP_016865456.1:p.Gln5771Ter
XM_017009968.2:c.17227C>T	XP_016865457.1:p.Gln5743Ter
XM_017009969.2:c.17407C>T	XP_016865458.1:p.Gln5803Ter
XM_017009972.1:c.10525C>T	XP_016865461.1:p.Gln3509Ter
XM_017009973.1:c.10504C>T	XP_016865462.1:p.Gln3502Ter