Canonical Allele Identifier: CA360399012

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90085627T>G (hg19) ; chr5:g.90789810T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789810T>G , CM000667.2:g.90789810T>G	GRCh38
NC_000005.9:g.90085627T>G , CM000667.1:g.90085627T>G	GRCh37
NC_000005.8:g.90121383T>G	NCBI36
NG_007083.1:g.236011T>G
NG_007083.2:g.265467T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14002T>G MANE Select	ENSP00000384582.2:p.Phe4668Val
ENST00000425867.3:c.2956T>G	ENSP00000392618.3:p.Phe986Val
ENST00000638510.1:n.1269T>G
ENST00000638975.1:c.631T>G	ENSP00000492630.1:p.Phe211Val
ENST00000639431.1:c.265+113601T>G	ENSP00000491057.1:n.265+113601T>G
ENST00000640407.1:c.412T>G	ENSP00000491425.1:p.Phe138Val
ENST00000405460.6:c.14002T>G	ENSP00000384582.2:p.Phe4668Val
ENST00000425867.2:c.985T>G	ENSP00000392618.2:p.Phe329Val
NM_032119.3:c.14002T>G	NP_115495.3:p.Phe4668Val
NR_003149.1:n.14015T>G
XM_011543675.1:c.13999T>G	XP_011541977.1:p.Phe4667Val
XM_011543676.1:c.13921T>G	XP_011541978.1:p.Phe4641Val
XM_011543677.1:c.11305T>G	XP_011541979.1:p.Phe3769Val
XM_011543678.1:c.14002T>G	XP_011541980.1:p.Phe4668Val
NM_032119.4:c.14002T>G MANE Select	NP_115495.3:p.Phe4668Val
XM_017009963.2:c.14023T>G	XP_016865452.1:p.Phe4675Val
XM_017009964.2:c.14020T>G	XP_016865453.1:p.Phe4674Val
XM_017009965.1:c.14020T>G	XP_016865454.1:p.Phe4674Val
XM_017009966.2:c.13942T>G	XP_016865455.1:p.Phe4648Val
XM_017009967.1:c.13927T>G	XP_016865456.1:p.Phe4643Val
XM_017009968.2:c.14023T>G	XP_016865457.1:p.Phe4675Val
XM_017009969.2:c.14023T>G	XP_016865458.1:p.Phe4675Val
XM_017009970.2:c.14023T>G	XP_016865459.1:p.Phe4675Val
XM_017009971.2:c.14023T>G	XP_016865460.1:p.Phe4675Val
XM_017009972.1:c.7141T>G	XP_016865461.1:p.Phe2381Val
XM_017009973.1:c.7120T>G	XP_016865462.1:p.Phe2374Val
NR_003149.2:n.14018T>G