Canonical Allele Identifier: CA360404837

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90728933-G-T
• MyVariant Identifiers: chr5:g.90024750G>T (hg19) ; chr5:g.90728933G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728933G>T , CM000667.2:g.90728933G>T	GRCh38
NC_000005.9:g.90024750G>T , CM000667.1:g.90024750G>T	GRCh37
NC_000005.8:g.90060506G>T	NCBI36
NG_007083.1:g.175134G>T
NG_007083.2:g.204590G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10426G>T MANE Select	ENSP00000384582.2:p.Gly3476Ter
ENST00000639431.1:c.265+52724G>T	ENSP00000491057.1:n.265+52724G>T
ENST00000640374.1:n.3570G>T
ENST00000640464.1:n.845G>T
ENST00000405460.6:c.10426G>T	ENSP00000384582.2:p.Gly3476Ter
ENST00000509621.1:c.3123G>T
NM_032119.3:c.10426G>T	NP_115495.3:p.Gly3476Ter
NR_003149.1:n.10439G>T
XM_011543675.1:c.10423G>T	XP_011541977.1:p.Gly3475Ter
XM_011543676.1:c.10345G>T	XP_011541978.1:p.Gly3449Ter
XM_011543677.1:c.7729G>T	XP_011541979.1:p.Gly2577Ter
XM_011543678.1:c.10426G>T	XP_011541980.1:p.Gly3476Ter
XM_011543679.1:c.10426G>T	XP_011541981.1:p.Gly3476Ter
XR_948560.1:n.271+11974C>A
NM_032119.4:c.10426G>T MANE Select	NP_115495.3:p.Gly3476Ter
XM_017009963.2:c.10447G>T	XP_016865452.1:p.Gly3483Ter
XM_017009964.2:c.10444G>T	XP_016865453.1:p.Gly3482Ter
XM_017009965.1:c.10444G>T	XP_016865454.1:p.Gly3482Ter
XM_017009966.2:c.10366G>T	XP_016865455.1:p.Gly3456Ter
XM_017009967.1:c.10351G>T	XP_016865456.1:p.Gly3451Ter
XM_017009968.2:c.10447G>T	XP_016865457.1:p.Gly3483Ter
XM_017009969.2:c.10447G>T	XP_016865458.1:p.Gly3483Ter
XM_017009970.2:c.10447G>T	XP_016865459.1:p.Gly3483Ter
XM_017009971.2:c.10447G>T	XP_016865460.1:p.Gly3483Ter
XM_017009972.1:c.3565G>T	XP_016865461.1:p.Gly1189Ter
XM_017009973.1:c.3544G>T	XP_016865462.1:p.Gly1182Ter
XM_017009974.2:c.10447G>T	XP_016865463.1:p.Gly3483Ter
XR_001742802.1:n.2522+11974C>A
NR_003149.2:n.10442G>T