Canonical Allele Identifier: CA360425576

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119310A>G (hg19) ; chr5:g.90823493A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823493A>G , CM000667.2:g.90823493A>G	GRCh38
NC_000005.9:g.90119310A>G , CM000667.1:g.90119310A>G	GRCh37
NC_000005.8:g.90155066A>G	NCBI36
NG_007083.1:g.269694A>G
NG_007083.2:g.299150A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16265A>G MANE Select	ENSP00000384582.2:p.Asp5422Gly
ENST00000425867.3:c.5219A>G	ENSP00000392618.3:p.Asp1740Gly
ENST00000638510.1:n.3532A>G
ENST00000639431.1:c.265+147284A>G	ENSP00000491057.1:n.265+147284A>G
ENST00000640061.1:n.128+1311A>G
ENST00000640407.1:c.2675A>G	ENSP00000491425.1:p.Asp892Gly
ENST00000405460.6:c.16265A>G	ENSP00000384582.2:p.Asp5422Gly
ENST00000425867.2:c.3248A>G	ENSP00000392618.2:p.Asp1083Gly
NM_032119.3:c.16265A>G	NP_115495.3:p.Asp5422Gly
NR_003149.1:n.16278A>G
XM_011543675.1:c.16262A>G	XP_011541977.1:p.Asp5421Gly
XM_011543676.1:c.16184A>G	XP_011541978.1:p.Asp5395Gly
XM_011543677.1:c.13568A>G	XP_011541979.1:p.Asp4523Gly
NM_032119.4:c.16265A>G MANE Select	NP_115495.3:p.Asp5422Gly
XM_017009963.2:c.16286A>G	XP_016865452.1:p.Asp5429Gly
XM_017009964.2:c.16283A>G	XP_016865453.1:p.Asp5428Gly
XM_017009965.1:c.16283A>G	XP_016865454.1:p.Asp5428Gly
XM_017009966.2:c.16205A>G	XP_016865455.1:p.Asp5402Gly
XM_017009967.1:c.16190A>G	XP_016865456.1:p.Asp5397Gly
XM_017009968.2:c.16106A>G	XP_016865457.1:p.Asp5369Gly
XM_017009969.2:c.16286A>G	XP_016865458.1:p.Asp5429Gly
XM_017009972.1:c.9404A>G	XP_016865461.1:p.Asp3135Gly
XM_017009973.1:c.9383A>G	XP_016865462.1:p.Asp3128Gly
NR_003149.2:n.16281A>G