Canonical Allele Identifier: CA223819

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811219A>T , CM000667.2:g.90811219A>T	GRCh38
NC_000005.9:g.90107036A>T , CM000667.1:g.90107036A>T	GRCh37
NC_000005.8:g.90142792A>T	NCBI36
NG_007083.1:g.257420A>T
NG_007083.2:g.286876A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15959A>T MANE Select	NP_115495.3:p.Asp5320Val
ENST00000405460.9:c.15959A>T MANE Select	ENSP00000384582.2:p.Asp5320Val
NM_032119.3:c.15959A>T	NP_115495.3:p.Asp5320Val
NR_003149.1:n.15972A>T
NR_003149.2:n.15975A>T
ENST00000405460.6:c.15959A>T	ENSP00000384582.2:p.Asp5320Val
ENST00000425867.2:c.2942A>T	ENSP00000392618.2:p.Asp981Val
ENST00000425867.3:c.4913A>T	ENSP00000392618.3:p.Asp1638Val
ENST00000638510.1:n.3226A>T
ENST00000639431.1:c.265+135010A>T	ENSP00000491057.1:n.265+135010A>T
ENST00000640407.1:c.2369A>T	ENSP00000491425.1:p.Asp790Val
XM_011543675.1:c.15956A>T	XP_011541977.1:p.Asp5319Val
XM_011543676.1:c.15878A>T	XP_011541978.1:p.Asp5293Val
XM_011543677.1:c.13262A>T	XP_011541979.1:p.Asp4421Val
XM_017009963.2:c.15980A>T	XP_016865452.1:p.Asp5327Val
XM_017009964.2:c.15977A>T	XP_016865453.1:p.Asp5326Val
XM_017009965.1:c.15977A>T	XP_016865454.1:p.Asp5326Val
XM_017009966.2:c.15899A>T	XP_016865455.1:p.Asp5300Val
XM_017009967.1:c.15884A>T	XP_016865456.1:p.Asp5295Val
XM_017009968.2:c.15800A>T	XP_016865457.1:p.Asp5267Val
XM_017009969.2:c.15980A>T	XP_016865458.1:p.Asp5327Val
XM_017009972.1:c.9098A>T	XP_016865461.1:p.Asp3033Val
XM_017009973.1:c.9077A>T	XP_016865462.1:p.Asp3026Val