Canonical Allele Identifier: CA360396162

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008127A>C (hg19) ; chr5:g.90712310A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712310A>C , CM000667.2:g.90712310A>C	GRCh38
NC_000005.9:g.90008127A>C , CM000667.1:g.90008127A>C	GRCh37
NC_000005.8:g.90043883A>C	NCBI36
NG_007083.1:g.158511A>C
NG_007083.2:g.187967A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9066A>C MANE Select	ENSP00000384582.2:p.Glu3022Asp
ENST00000639431.1:c.265+36101A>C	ENSP00000491057.1:n.265+36101A>C
ENST00000639473.1:n.4525A>C
ENST00000640012.1:c.2873A>C
ENST00000640374.1:n.2210A>C
ENST00000640779.1:c.3795A>C
ENST00000405460.6:c.9066A>C	ENSP00000384582.2:p.Glu3022Asp
ENST00000509621.1:c.1763A>C
NM_032119.3:c.9066A>C	NP_115495.3:p.Glu3022Asp
NR_003149.1:n.9079A>C
XM_011543675.1:c.9063A>C	XP_011541977.1:p.Glu3021Asp
XM_011543676.1:c.8985A>C	XP_011541978.1:p.Glu2995Asp
XM_011543677.1:c.6369A>C	XP_011541979.1:p.Glu2123Asp
XM_011543678.1:c.9066A>C	XP_011541980.1:p.Glu3022Asp
XM_011543679.1:c.9066A>C	XP_011541981.1:p.Glu3022Asp
NM_032119.4:c.9066A>C MANE Select	NP_115495.3:p.Glu3022Asp
XM_017009963.2:c.9087A>C	XP_016865452.1:p.Glu3029Asp
XM_017009964.2:c.9084A>C	XP_016865453.1:p.Glu3028Asp
XM_017009965.1:c.9084A>C	XP_016865454.1:p.Glu3028Asp
XM_017009966.2:c.9006A>C	XP_016865455.1:p.Glu3002Asp
XM_017009967.1:c.8991A>C	XP_016865456.1:p.Glu2997Asp
XM_017009968.2:c.9087A>C	XP_016865457.1:p.Glu3029Asp
XM_017009969.2:c.9087A>C	XP_016865458.1:p.Glu3029Asp
XM_017009970.2:c.9087A>C	XP_016865459.1:p.Glu3029Asp
XM_017009971.2:c.9087A>C	XP_016865460.1:p.Glu3029Asp
XM_017009972.1:c.2205A>C	XP_016865461.1:p.Glu735Asp
XM_017009973.1:c.2184A>C	XP_016865462.1:p.Glu728Asp
XM_017009974.2:c.9087A>C	XP_016865463.1:p.Glu3029Asp
NR_003149.2:n.9082A>C