Canonical Allele Identifier: CA2767421064

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728994_90728995insA , CM000667.2:g.90728994_90728995insA	GRCh38
NC_000005.9:g.90024811_90024812insA , CM000667.1:g.90024811_90024812insA	GRCh37
NC_000005.8:g.90060567_90060568insA	NCBI36
NG_007083.1:g.175195_175196insA
NG_007083.2:g.204651_204652insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10426+61_10426+62insA MANE Select	ENSP00000384582.2:n.10426+61_10426+62insA
ENST00000639431.1:c.265+52785_265+52786insA	ENSP00000491057.1:n.265+52785_265+52786insA
ENST00000640374.1:n.3570+61_3570+62insA
ENST00000640464.1:n.845+61_845+62insA
ENST00000405460.6:c.10426+61_10426+62insA	ENSP00000384582.2:n.10426+61_10426+62insA
ENST00000509621.1:c.3123+61_3123+62insA
NM_032119.3:c.10426+61_10426+62insA	NP_115495.3:n.10426+61_10426+62insA
NR_003149.1:n.10439+61_10439+62insA
XM_011543675.1:c.10423+61_10423+62insA	XP_011541977.1:n.10423+61_10423+62insA
XM_011543676.1:c.10345+61_10345+62insA	XP_011541978.1:n.10345+61_10345+62insA
XM_011543677.1:c.7729+61_7729+62insA	XP_011541979.1:n.7729+61_7729+62insA
XM_011543678.1:c.10426+61_10426+62insA	XP_011541980.1:n.10426+61_10426+62insA
XM_011543679.1:c.10426+61_10426+62insA	XP_011541981.1:n.10426+61_10426+62insA
XR_948560.1:n.271+11912_271+11913insT
NM_032119.4:c.10426+61_10426+62insA MANE Select	NP_115495.3:n.10426+61_10426+62insA
XM_017009963.2:c.10447+61_10447+62insA	XP_016865452.1:n.10447+61_10447+62insA
XM_017009964.2:c.10444+61_10444+62insA	XP_016865453.1:n.10444+61_10444+62insA
XM_017009965.1:c.10444+61_10444+62insA	XP_016865454.1:n.10444+61_10444+62insA
XM_017009966.2:c.10366+61_10366+62insA	XP_016865455.1:n.10366+61_10366+62insA
XM_017009967.1:c.10351+61_10351+62insA	XP_016865456.1:n.10351+61_10351+62insA
XM_017009968.2:c.10447+61_10447+62insA	XP_016865457.1:n.10447+61_10447+62insA
XM_017009969.2:c.10447+61_10447+62insA	XP_016865458.1:n.10447+61_10447+62insA
XM_017009970.2:c.10447+61_10447+62insA	XP_016865459.1:n.10447+61_10447+62insA
XM_017009971.2:c.10447+61_10447+62insA	XP_016865460.1:n.10447+61_10447+62insA
XM_017009972.1:c.3565+61_3565+62insA	XP_016865461.1:n.3565+61_3565+62insA
XM_017009973.1:c.3544+61_3544+62insA	XP_016865462.1:n.3544+61_3544+62insA
XM_017009974.2:c.10447+61_10447+62insA	XP_016865463.1:n.10447+61_10447+62insA
XR_001742802.1:n.2522+11912_2522+11913insT
NR_003149.2:n.10442+61_10442+62insA