Canonical Allele Identifier: CA122809900

Gene: ADGRV1

Linked Data

• dbSNP Id: rs527703074
• gnomAD v2: 5-90024882-TATTA-T
• gnomAD v3: 5-90729065-TATTA-T
• gnomAD v4: 5-90729065-TATTA-T
• MyVariant Identifiers: chr5:g.90024883_90024886del (hg19) ; chr5:g.90729066_90729069del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90729069_90729072del , CM000667.2:g.90729069_90729072del	GRCh38
NC_000005.9:g.90024886_90024889del , CM000667.1:g.90024886_90024889del	GRCh37
NC_000005.8:g.90060642_90060645del	NCBI36
NG_007083.1:g.175270_175273del
NG_007083.2:g.204726_204729del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10426+136_10426+139del MANE Select	ENSP00000384582.2:n.10426+136_10426+139del
ENST00000639431.1:c.265+52860_265+52863del	ENSP00000491057.1:n.265+52860_265+52863del
ENST00000640374.1:n.3570+136_3570+139del
ENST00000640464.1:n.845+136_845+139del
ENST00000405460.6:c.10426+136_10426+139del	ENSP00000384582.2:n.10426+136_10426+139del
ENST00000509621.1:c.3123+136_3123+139del
NM_032119.3:c.10426+136_10426+139del	NP_115495.3:n.10426+136_10426+139del
NR_003149.1:n.10439+136_10439+139del
XM_011543675.1:c.10423+136_10423+139del	XP_011541977.1:n.10423+136_10423+139del
XM_011543676.1:c.10345+136_10345+139del	XP_011541978.1:n.10345+136_10345+139del
XM_011543677.1:c.7729+136_7729+139del	XP_011541979.1:n.7729+136_7729+139del
XM_011543678.1:c.10426+136_10426+139del	XP_011541980.1:n.10426+136_10426+139del
XM_011543679.1:c.10426+136_10426+139del	XP_011541981.1:n.10426+136_10426+139del
XR_948560.1:n.271+11838_271+11841del
NM_032119.4:c.10426+136_10426+139del MANE Select	NP_115495.3:n.10426+136_10426+139del
XM_017009963.2:c.10447+136_10447+139del	XP_016865452.1:n.10447+136_10447+139del
XM_017009964.2:c.10444+136_10444+139del	XP_016865453.1:n.10444+136_10444+139del
XM_017009965.1:c.10444+136_10444+139del	XP_016865454.1:n.10444+136_10444+139del
XM_017009966.2:c.10366+136_10366+139del	XP_016865455.1:n.10366+136_10366+139del
XM_017009967.1:c.10351+136_10351+139del	XP_016865456.1:n.10351+136_10351+139del
XM_017009968.2:c.10447+136_10447+139del	XP_016865457.1:n.10447+136_10447+139del
XM_017009969.2:c.10447+136_10447+139del	XP_016865458.1:n.10447+136_10447+139del
XM_017009970.2:c.10447+136_10447+139del	XP_016865459.1:n.10447+136_10447+139del
XM_017009971.2:c.10447+136_10447+139del	XP_016865460.1:n.10447+136_10447+139del
XM_017009972.1:c.3565+136_3565+139del	XP_016865461.1:n.3565+136_3565+139del
XM_017009973.1:c.3544+136_3544+139del	XP_016865462.1:n.3544+136_3544+139del
XM_017009974.2:c.10447+136_10447+139del	XP_016865463.1:n.10447+136_10447+139del
XR_001742802.1:n.2522+11838_2522+11841del
NR_003149.2:n.10442+136_10442+139del