Canonical Allele Identifier: CA3341986

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811089C>T , CM000667.2:g.90811089C>T	GRCh38
NC_000005.9:g.90106906C>T , CM000667.1:g.90106906C>T	GRCh37
NC_000005.8:g.90142662C>T	NCBI36
NG_007083.1:g.257290C>T
NG_007083.2:g.286746C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15829C>T MANE Select	NP_115495.3:p.Arg5277Cys
ENST00000405460.9:c.15829C>T MANE Select	ENSP00000384582.2:p.Arg5277Cys
NM_032119.3:c.15829C>T	NP_115495.3:p.Arg5277Cys
NR_003149.1:n.15842C>T
NR_003149.2:n.15845C>T
ENST00000405460.6:c.15829C>T	ENSP00000384582.2:p.Arg5277Cys
ENST00000425867.2:c.2812C>T	ENSP00000392618.2:p.Arg938Cys
ENST00000425867.3:c.4783C>T	ENSP00000392618.3:p.Arg1595Cys
ENST00000638510.1:n.3096C>T
ENST00000639431.1:c.265+134880C>T	ENSP00000491057.1:n.265+134880C>T
ENST00000640407.1:c.2239C>T	ENSP00000491425.1:p.Arg747Cys
XM_011543675.1:c.15826C>T	XP_011541977.1:p.Arg5276Cys
XM_011543676.1:c.15748C>T	XP_011541978.1:p.Arg5250Cys
XM_011543677.1:c.13132C>T	XP_011541979.1:p.Arg4378Cys
XM_017009963.2:c.15850C>T	XP_016865452.1:p.Arg5284Cys
XM_017009964.2:c.15847C>T	XP_016865453.1:p.Arg5283Cys
XM_017009965.1:c.15847C>T	XP_016865454.1:p.Arg5283Cys
XM_017009966.2:c.15769C>T	XP_016865455.1:p.Arg5257Cys
XM_017009967.1:c.15754C>T	XP_016865456.1:p.Arg5252Cys
XM_017009968.2:c.15670C>T	XP_016865457.1:p.Arg5224Cys
XM_017009969.2:c.15850C>T	XP_016865458.1:p.Arg5284Cys
XM_017009972.1:c.8968C>T	XP_016865461.1:p.Arg2990Cys
XM_017009973.1:c.8947C>T	XP_016865462.1:p.Arg2983Cys