Canonical Allele Identifier: CA360404832

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90024750G>C (hg19) ; chr5:g.90728933G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10426G>C MANE Select	ENSP00000384582.2:p.Gly3476Arg
ENST00000639431.1:c.265+52724G>C	ENSP00000491057.1:n.265+52724G>C
ENST00000640374.1:n.3570G>C
ENST00000640464.1:n.845G>C
ENST00000405460.6:c.10426G>C	ENSP00000384582.2:p.Gly3476Arg
ENST00000509621.1:c.3123G>C
NM_032119.3:c.10426G>C	NP_115495.3:p.Gly3476Arg
NR_003149.1:n.10439G>C
XM_011543675.1:c.10423G>C	XP_011541977.1:p.Gly3475Arg
XM_011543676.1:c.10345G>C	XP_011541978.1:p.Gly3449Arg
XM_011543677.1:c.7729G>C	XP_011541979.1:p.Gly2577Arg
XM_011543678.1:c.10426G>C	XP_011541980.1:p.Gly3476Arg
XM_011543679.1:c.10426G>C	XP_011541981.1:p.Gly3476Arg
XR_948560.1:n.271+11974C>G
NM_032119.4:c.10426G>C MANE Select	NP_115495.3:p.Gly3476Arg
XM_017009963.2:c.10447G>C	XP_016865452.1:p.Gly3483Arg
XM_017009964.2:c.10444G>C	XP_016865453.1:p.Gly3482Arg
XM_017009965.1:c.10444G>C	XP_016865454.1:p.Gly3482Arg
XM_017009966.2:c.10366G>C	XP_016865455.1:p.Gly3456Arg
XM_017009967.1:c.10351G>C	XP_016865456.1:p.Gly3451Arg
XM_017009968.2:c.10447G>C	XP_016865457.1:p.Gly3483Arg
XM_017009969.2:c.10447G>C	XP_016865458.1:p.Gly3483Arg
XM_017009970.2:c.10447G>C	XP_016865459.1:p.Gly3483Arg
XM_017009971.2:c.10447G>C	XP_016865460.1:p.Gly3483Arg
XM_017009972.1:c.3565G>C	XP_016865461.1:p.Gly1189Arg
XM_017009973.1:c.3544G>C	XP_016865462.1:p.Gly1182Arg
XM_017009974.2:c.10447G>C	XP_016865463.1:p.Gly3483Arg
XR_001742802.1:n.2522+11974C>G
NR_003149.2:n.10442G>C