Canonical Allele Identifier: CA360425496

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119267T>G (hg19) ; chr5:g.90823450T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823450T>G , CM000667.2:g.90823450T>G	GRCh38
NC_000005.9:g.90119267T>G , CM000667.1:g.90119267T>G	GRCh37
NC_000005.8:g.90155023T>G	NCBI36
NG_007083.1:g.269651T>G
NG_007083.2:g.299107T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16222T>G MANE Select	ENSP00000384582.2:p.Trp5408Gly
ENST00000425867.3:c.5176T>G	ENSP00000392618.3:p.Trp1726Gly
ENST00000638510.1:n.3489T>G
ENST00000639431.1:c.265+147241T>G	ENSP00000491057.1:n.265+147241T>G
ENST00000640061.1:n.128+1268T>G
ENST00000640407.1:c.2632T>G	ENSP00000491425.1:p.Trp878Gly
ENST00000405460.6:c.16222T>G	ENSP00000384582.2:p.Trp5408Gly
ENST00000425867.2:c.3205T>G	ENSP00000392618.2:p.Trp1069Gly
NM_032119.3:c.16222T>G	NP_115495.3:p.Trp5408Gly
NR_003149.1:n.16235T>G
XM_011543675.1:c.16219T>G	XP_011541977.1:p.Trp5407Gly
XM_011543676.1:c.16141T>G	XP_011541978.1:p.Trp5381Gly
XM_011543677.1:c.13525T>G	XP_011541979.1:p.Trp4509Gly
NM_032119.4:c.16222T>G MANE Select	NP_115495.3:p.Trp5408Gly
XM_017009963.2:c.16243T>G	XP_016865452.1:p.Trp5415Gly
XM_017009964.2:c.16240T>G	XP_016865453.1:p.Trp5414Gly
XM_017009965.1:c.16240T>G	XP_016865454.1:p.Trp5414Gly
XM_017009966.2:c.16162T>G	XP_016865455.1:p.Trp5388Gly
XM_017009967.1:c.16147T>G	XP_016865456.1:p.Trp5383Gly
XM_017009968.2:c.16063T>G	XP_016865457.1:p.Trp5355Gly
XM_017009969.2:c.16243T>G	XP_016865458.1:p.Trp5415Gly
XM_017009972.1:c.9361T>G	XP_016865461.1:p.Trp3121Gly
XM_017009973.1:c.9340T>G	XP_016865462.1:p.Trp3114Gly
NR_003149.2:n.16238T>G