Canonical Allele Identifier: CA360403800

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90024546C>A (hg19) ; chr5:g.90728729C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728729C>A , CM000667.2:g.90728729C>A	GRCh38
NC_000005.9:g.90024546C>A , CM000667.1:g.90024546C>A	GRCh37
NC_000005.8:g.90060302C>A	NCBI36
NG_007083.1:g.174930C>A
NG_007083.2:g.204386C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10222C>A MANE Select	ENSP00000384582.2:p.Leu3408Met
ENST00000639431.1:c.265+52520C>A	ENSP00000491057.1:n.265+52520C>A
ENST00000640374.1:n.3366C>A
ENST00000640464.1:n.641C>A
ENST00000405460.6:c.10222C>A	ENSP00000384582.2:p.Leu3408Met
ENST00000509621.1:c.2919C>A
NM_032119.3:c.10222C>A	NP_115495.3:p.Leu3408Met
NR_003149.1:n.10235C>A
XM_011543675.1:c.10219C>A	XP_011541977.1:p.Leu3407Met
XM_011543676.1:c.10141C>A	XP_011541978.1:p.Leu3381Met
XM_011543677.1:c.7525C>A	XP_011541979.1:p.Leu2509Met
XM_011543678.1:c.10222C>A	XP_011541980.1:p.Leu3408Met
XM_011543679.1:c.10222C>A	XP_011541981.1:p.Leu3408Met
XR_948560.1:n.271+12178G>T
NM_032119.4:c.10222C>A MANE Select	NP_115495.3:p.Leu3408Met
XM_017009963.2:c.10243C>A	XP_016865452.1:p.Leu3415Met
XM_017009964.2:c.10240C>A	XP_016865453.1:p.Leu3414Met
XM_017009965.1:c.10240C>A	XP_016865454.1:p.Leu3414Met
XM_017009966.2:c.10162C>A	XP_016865455.1:p.Leu3388Met
XM_017009967.1:c.10147C>A	XP_016865456.1:p.Leu3383Met
XM_017009968.2:c.10243C>A	XP_016865457.1:p.Leu3415Met
XM_017009969.2:c.10243C>A	XP_016865458.1:p.Leu3415Met
XM_017009970.2:c.10243C>A	XP_016865459.1:p.Leu3415Met
XM_017009971.2:c.10243C>A	XP_016865460.1:p.Leu3415Met
XM_017009972.1:c.3361C>A	XP_016865461.1:p.Leu1121Met
XM_017009973.1:c.3340C>A	XP_016865462.1:p.Leu1114Met
XM_017009974.2:c.10243C>A	XP_016865463.1:p.Leu3415Met
XR_001742802.1:n.2522+12178G>T
NR_003149.2:n.10238C>A