Canonical Allele Identifier: CA360403191

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90021380T>G (hg19) ; chr5:g.90725563T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725563T>G , CM000667.2:g.90725563T>G	GRCh38
NC_000005.9:g.90021380T>G , CM000667.1:g.90021380T>G	GRCh37
NC_000005.8:g.90057136T>G	NCBI36
NG_007083.1:g.171764T>G
NG_007083.2:g.201220T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10068T>G MANE Select	ENSP00000384582.2:p.Ile3356Met
ENST00000639431.1:c.265+49354T>G	ENSP00000491057.1:n.265+49354T>G
ENST00000640374.1:n.3212T>G
ENST00000640464.1:n.487T>G
ENST00000405460.6:c.10068T>G	ENSP00000384582.2:p.Ile3356Met
ENST00000509621.1:c.2765T>G
NM_032119.3:c.10068T>G	NP_115495.3:p.Ile3356Met
NR_003149.1:n.10081T>G
XM_011543675.1:c.10065T>G	XP_011541977.1:p.Ile3355Met
XM_011543676.1:c.9987T>G	XP_011541978.1:p.Ile3329Met
XM_011543677.1:c.7371T>G	XP_011541979.1:p.Ile2457Met
XM_011543678.1:c.10068T>G	XP_011541980.1:p.Ile3356Met
XM_011543679.1:c.10068T>G	XP_011541981.1:p.Ile3356Met
XR_948560.1:n.272-9754A>C
NM_032119.4:c.10068T>G MANE Select	NP_115495.3:p.Ile3356Met
XM_017009963.2:c.10089T>G	XP_016865452.1:p.Ile3363Met
XM_017009964.2:c.10086T>G	XP_016865453.1:p.Ile3362Met
XM_017009965.1:c.10086T>G	XP_016865454.1:p.Ile3362Met
XM_017009966.2:c.10008T>G	XP_016865455.1:p.Ile3336Met
XM_017009967.1:c.9993T>G	XP_016865456.1:p.Ile3331Met
XM_017009968.2:c.10089T>G	XP_016865457.1:p.Ile3363Met
XM_017009969.2:c.10089T>G	XP_016865458.1:p.Ile3363Met
XM_017009970.2:c.10089T>G	XP_016865459.1:p.Ile3363Met
XM_017009971.2:c.10089T>G	XP_016865460.1:p.Ile3363Met
XM_017009972.1:c.3207T>G	XP_016865461.1:p.Ile1069Met
XM_017009973.1:c.3186T>G	XP_016865462.1:p.Ile1062Met
XM_017009974.2:c.10089T>G	XP_016865463.1:p.Ile3363Met
XR_001742802.1:n.2523-9754A>C
NR_003149.2:n.10084T>G