Canonical Allele Identifier: CA360426925

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90965508C>T , CM000667.2:g.90965508C>T	GRCh38
NC_000005.9:g.90261325C>T , CM000667.1:g.90261325C>T	GRCh37
NC_000005.8:g.90297081C>T	NCBI36
NG_007083.1:g.411709C>T
NG_007083.2:g.441165C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17950C>T MANE Select	NP_115495.3:p.Gln5984Ter
ENST00000405460.9:c.17950C>T MANE Select	ENSP00000384582.2:p.Gln5984Ter
NM_032119.3:c.17950C>T	NP_115495.3:p.Gln5984Ter
NR_003149.1:n.17963C>T
NR_003149.2:n.17966C>T
ENST00000405460.6:c.17950C>T	ENSP00000384582.2:p.Gln5984Ter
ENST00000425867.2:c.4933C>T	ENSP00000392618.2:p.Gln1645Ter
ENST00000425867.3:c.6904C>T	ENSP00000392618.3:p.Gln2302Ter
ENST00000638510.1:n.5217C>T
ENST00000638990.1:c.1162C>T
ENST00000639431.1:c.266-19836C>T	ENSP00000491057.1:n.266-19836C>T
ENST00000639707.1:c.34C>T	ENSP00000492328.1:p.Gln12Ter
ENST00000639821.1:c.34C>T	ENSP00000492216.1:p.Gln12Ter
ENST00000640369.1:c.34C>T	ENSP00000491401.1:p.Gln12Ter
ENST00000640407.1:c.4399C>T	ENSP00000491425.1:n.4399C>T
ENST00000640815.1:c.34C>T	ENSP00000491767.1:p.Gln12Ter
XM_011543675.1:c.17947C>T	XP_011541977.1:p.Gln5983Ter
XM_011543676.1:c.17869C>T	XP_011541978.1:p.Gln5957Ter
XM_011543677.1:c.15253C>T	XP_011541979.1:p.Gln5085Ter
XM_017009963.2:c.17971C>T	XP_016865452.1:p.Gln5991Ter
XM_017009964.2:c.17968C>T	XP_016865453.1:p.Gln5990Ter
XM_017009965.1:c.17968C>T	XP_016865454.1:p.Gln5990Ter
XM_017009966.2:c.17890C>T	XP_016865455.1:p.Gln5964Ter
XM_017009967.1:c.17875C>T	XP_016865456.1:p.Gln5959Ter
XM_017009968.2:c.17791C>T	XP_016865457.1:p.Gln5931Ter
XM_017009969.2:c.17971C>T	XP_016865458.1:p.Gln5991Ter
XM_017009972.1:c.11089C>T	XP_016865461.1:p.Gln3697Ter
XM_017009973.1:c.11068C>T	XP_016865462.1:p.Gln3690Ter