Canonical Allele Identifier: CA560901863

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1489892001
• gnomAD v2: 5-90024759-ATAAAG-A
• gnomAD v3: 5-90728942-ATAAAG-A
• gnomAD v4: 5-90728942-ATAAAG-A
• MyVariant Identifiers: chr5:g.90024760_90024764del (hg19) ; chr5:g.90728943_90728947del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728945_90728949del , CM000667.2:g.90728945_90728949del	GRCh38
NC_000005.9:g.90024762_90024766del , CM000667.1:g.90024762_90024766del	GRCh37
NC_000005.8:g.90060518_90060522del	NCBI36
NG_007083.1:g.175146_175150del
NG_007083.2:g.204602_204606del

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10426+12_10426+16del MANE Select	ENSP00000384582.2:n.10426+12_10426+16del
ENST00000639431.1:c.265+52736_265+52740del	ENSP00000491057.1:n.265+52736_265+52740de...
ENST00000640374.1:n.3570+12_3570+16del
ENST00000640464.1:n.845+12_845+16del
ENST00000405460.6:c.10426+12_10426+16del	ENSP00000384582.2:n.10426+12_10426+16del
ENST00000509621.1:c.3123+12_3123+16del
NM_032119.3:c.10426+12_10426+16del	NP_115495.3:n.10426+12_10426+16del
NR_003149.1:n.10439+12_10439+16del
XM_011543675.1:c.10423+12_10423+16del	XP_011541977.1:n.10423+12_10423+16del
XM_011543676.1:c.10345+12_10345+16del	XP_011541978.1:n.10345+12_10345+16del
XM_011543677.1:c.7729+12_7729+16del	XP_011541979.1:n.7729+12_7729+16del
XM_011543678.1:c.10426+12_10426+16del	XP_011541980.1:n.10426+12_10426+16del
XM_011543679.1:c.10426+12_10426+16del	XP_011541981.1:n.10426+12_10426+16del
XR_948560.1:n.271+11960_271+11964del
NM_032119.4:c.10426+12_10426+16del MANE Select	NP_115495.3:n.10426+12_10426+16del
XM_017009963.2:c.10447+12_10447+16del	XP_016865452.1:n.10447+12_10447+16del
XM_017009964.2:c.10444+12_10444+16del	XP_016865453.1:n.10444+12_10444+16del
XM_017009965.1:c.10444+12_10444+16del	XP_016865454.1:n.10444+12_10444+16del
XM_017009966.2:c.10366+12_10366+16del	XP_016865455.1:n.10366+12_10366+16del
XM_017009967.1:c.10351+12_10351+16del	XP_016865456.1:n.10351+12_10351+16del
XM_017009968.2:c.10447+12_10447+16del	XP_016865457.1:n.10447+12_10447+16del
XM_017009969.2:c.10447+12_10447+16del	XP_016865458.1:n.10447+12_10447+16del
XM_017009970.2:c.10447+12_10447+16del	XP_016865459.1:n.10447+12_10447+16del
XM_017009971.2:c.10447+12_10447+16del	XP_016865460.1:n.10447+12_10447+16del
XM_017009972.1:c.3565+12_3565+16del	XP_016865461.1:n.3565+12_3565+16del
XM_017009973.1:c.3544+12_3544+16del	XP_016865462.1:n.3544+12_3544+16del
XM_017009974.2:c.10447+12_10447+16del	XP_016865463.1:n.10447+12_10447+16del
XR_001742802.1:n.2522+11960_2522+11964del
NR_003149.2:n.10442+12_10442+16del