Canonical Allele Identifier: CA360401260

Gene: ADGRV1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14276A>C MANE Select	ENSP00000384582.2:p.Asp4759Ala
ENST00000425867.3:c.3230A>C	ENSP00000392618.3:p.Asp1077Ala
ENST00000638510.1:n.1543A>C
ENST00000638585.1:n.42A>C
ENST00000638975.1:c.905A>C	ENSP00000492630.1:p.Asp302Ala
ENST00000639431.1:c.265+114896A>C	ENSP00000491057.1:n.265+114896A>C
ENST00000640407.1:c.686A>C	ENSP00000491425.1:p.Asp229Ala
ENST00000405460.6:c.14276A>C	ENSP00000384582.2:p.Asp4759Ala
ENST00000425867.2:c.1259A>C	ENSP00000392618.2:p.Asp420Ala
NM_032119.3:c.14276A>C	NP_115495.3:p.Asp4759Ala
NR_003149.1:n.14289A>C
XM_011543675.1:c.14273A>C	XP_011541977.1:p.Asp4758Ala
XM_011543676.1:c.14195A>C	XP_011541978.1:p.Asp4732Ala
XM_011543677.1:c.11579A>C	XP_011541979.1:p.Asp3860Ala
XM_011543678.1:c.14276A>C	XP_011541980.1:p.Asp4759Ala
NM_032119.4:c.14276A>C MANE Select	NP_115495.3:p.Asp4759Ala
XM_017009963.2:c.14297A>C	XP_016865452.1:p.Asp4766Ala
XM_017009964.2:c.14294A>C	XP_016865453.1:p.Asp4765Ala
XM_017009965.1:c.14294A>C	XP_016865454.1:p.Asp4765Ala
XM_017009966.2:c.14216A>C	XP_016865455.1:p.Asp4739Ala
XM_017009967.1:c.14201A>C	XP_016865456.1:p.Asp4734Ala
XM_017009968.2:c.14297A>C	XP_016865457.1:p.Asp4766Ala
XM_017009969.2:c.14297A>C	XP_016865458.1:p.Asp4766Ala
XM_017009970.2:c.14297A>C	XP_016865459.1:p.Asp4766Ala
XM_017009971.2:c.14297A>C	XP_016865460.1:p.Asp4766Ala
XM_017009972.1:c.7415A>C	XP_016865461.1:p.Asp2472Ala
XM_017009973.1:c.7394A>C	XP_016865462.1:p.Asp2465Ala
NR_003149.2:n.14292A>C