Canonical Allele Identifier: CA360408952

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1327812030
• MyVariant Identifiers: chr5:g.90041453A>G (hg19) ; chr5:g.90745636A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745636A>G , CM000667.2:g.90745636A>G	GRCh38
NC_000005.9:g.90041453A>G , CM000667.1:g.90041453A>G	GRCh37
NC_000005.8:g.90077209A>G	NCBI36
NG_007083.1:g.191837A>G
NG_007083.2:g.221293A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10815A>G MANE Select	ENSP00000384582.2:p.Ile3605Met
ENST00000639431.1:c.265+69427A>G	ENSP00000491057.1:n.265+69427A>G
ENST00000640374.1:n.3959A>G
ENST00000640464.1:n.1234A>G
ENST00000405460.6:c.10815A>G	ENSP00000384582.2:p.Ile3605Met
ENST00000509621.1:c.3512A>G
NM_032119.3:c.10815A>G	NP_115495.3:p.Ile3605Met
NR_003149.1:n.10828A>G
XM_011543675.1:c.10812A>G	XP_011541977.1:p.Ile3604Met
XM_011543676.1:c.10734A>G	XP_011541978.1:p.Ile3578Met
XM_011543677.1:c.8118A>G	XP_011541979.1:p.Ile2706Met
XM_011543678.1:c.10815A>G	XP_011541980.1:p.Ile3605Met
XM_011543679.1:c.*37A>G	XP_011541981.1:n.*37A>G
NM_032119.4:c.10815A>G MANE Select	NP_115495.3:p.Ile3605Met
XM_017009963.2:c.10836A>G	XP_016865452.1:p.Ile3612Met
XM_017009964.2:c.10833A>G	XP_016865453.1:p.Ile3611Met
XM_017009965.1:c.10833A>G	XP_016865454.1:p.Ile3611Met
XM_017009966.2:c.10755A>G	XP_016865455.1:p.Ile3585Met
XM_017009967.1:c.10740A>G	XP_016865456.1:p.Ile3580Met
XM_017009968.2:c.10836A>G	XP_016865457.1:p.Ile3612Met
XM_017009969.2:c.10836A>G	XP_016865458.1:p.Ile3612Met
XM_017009970.2:c.10836A>G	XP_016865459.1:p.Ile3612Met
XM_017009971.2:c.10836A>G	XP_016865460.1:p.Ile3612Met
XM_017009972.1:c.3954A>G	XP_016865461.1:p.Ile1318Met
XM_017009973.1:c.3933A>G	XP_016865462.1:p.Ile1311Met
XM_017009974.2:c.*37A>G	XP_016865463.1:n.*37A>G
NR_003149.2:n.10831A>G