Canonical Allele Identifier: CA360401270

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086922A>T (hg19) ; chr5:g.90791105A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791105A>T , CM000667.2:g.90791105A>T	GRCh38
NC_000005.9:g.90086922A>T , CM000667.1:g.90086922A>T	GRCh37
NC_000005.8:g.90122678A>T	NCBI36
NG_007083.1:g.237306A>T
NG_007083.2:g.266762A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14276A>T MANE Select	ENSP00000384582.2:p.Asp4759Val
ENST00000425867.3:c.3230A>T	ENSP00000392618.3:p.Asp1077Val
ENST00000638510.1:n.1543A>T
ENST00000638585.1:n.42A>T
ENST00000638975.1:c.905A>T	ENSP00000492630.1:p.Asp302Val
ENST00000639431.1:c.265+114896A>T	ENSP00000491057.1:n.265+114896A>T
ENST00000640407.1:c.686A>T	ENSP00000491425.1:p.Asp229Val
ENST00000405460.6:c.14276A>T	ENSP00000384582.2:p.Asp4759Val
ENST00000425867.2:c.1259A>T	ENSP00000392618.2:p.Asp420Val
NM_032119.3:c.14276A>T	NP_115495.3:p.Asp4759Val
NR_003149.1:n.14289A>T
XM_011543675.1:c.14273A>T	XP_011541977.1:p.Asp4758Val
XM_011543676.1:c.14195A>T	XP_011541978.1:p.Asp4732Val
XM_011543677.1:c.11579A>T	XP_011541979.1:p.Asp3860Val
XM_011543678.1:c.14276A>T	XP_011541980.1:p.Asp4759Val
NM_032119.4:c.14276A>T MANE Select	NP_115495.3:p.Asp4759Val
XM_017009963.2:c.14297A>T	XP_016865452.1:p.Asp4766Val
XM_017009964.2:c.14294A>T	XP_016865453.1:p.Asp4765Val
XM_017009965.1:c.14294A>T	XP_016865454.1:p.Asp4765Val
XM_017009966.2:c.14216A>T	XP_016865455.1:p.Asp4739Val
XM_017009967.1:c.14201A>T	XP_016865456.1:p.Asp4734Val
XM_017009968.2:c.14297A>T	XP_016865457.1:p.Asp4766Val
XM_017009969.2:c.14297A>T	XP_016865458.1:p.Asp4766Val
XM_017009970.2:c.14297A>T	XP_016865459.1:p.Asp4766Val
XM_017009971.2:c.14297A>T	XP_016865460.1:p.Asp4766Val
XM_017009972.1:c.7415A>T	XP_016865461.1:p.Asp2472Val
XM_017009973.1:c.7394A>T	XP_016865462.1:p.Asp2465Val
NR_003149.2:n.14292A>T