Canonical Allele Identifier: CA360371948

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90692762-G-T
• MyVariant Identifiers: chr5:g.89988579G>T (hg19) ; chr5:g.90692762G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692762G>T , CM000667.2:g.90692762G>T	GRCh38
NC_000005.9:g.89988579G>T , CM000667.1:g.89988579G>T	GRCh37
NC_000005.8:g.90024335G>T	NCBI36
NG_007083.1:g.138963G>T
NG_007083.2:g.168419G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7109G>T MANE Select	ENSP00000384582.2:p.Cys2370Phe
ENST00000639431.1:c.265+16553G>T	ENSP00000491057.1:n.265+16553G>T
ENST00000639473.1:n.2568G>T
ENST00000640012.1:c.916G>T
ENST00000640374.1:n.253G>T
ENST00000640403.1:c.4400G>T	ENSP00000492531.1:p.Cys1467Phe
ENST00000640779.1:c.1838G>T
ENST00000405460.6:c.7109G>T	ENSP00000384582.2:p.Cys2370Phe
NM_032119.3:c.7109G>T	NP_115495.3:p.Cys2370Phe
NR_003149.1:n.7122G>T
XM_011543675.1:c.7106G>T	XP_011541977.1:p.Cys2369Phe
XM_011543676.1:c.7028G>T	XP_011541978.1:p.Cys2343Phe
XM_011543677.1:c.4412G>T	XP_011541979.1:p.Cys1471Phe
XM_011543678.1:c.7109G>T	XP_011541980.1:p.Cys2370Phe
XM_011543679.1:c.7109G>T	XP_011541981.1:p.Cys2370Phe
NM_032119.4:c.7109G>T MANE Select	NP_115495.3:p.Cys2370Phe
XM_017009963.2:c.7109G>T	XP_016865452.1:p.Cys2370Phe
XM_017009964.2:c.7106G>T	XP_016865453.1:p.Cys2369Phe
XM_017009965.1:c.7106G>T	XP_016865454.1:p.Cys2369Phe
XM_017009966.2:c.7028G>T	XP_016865455.1:p.Cys2343Phe
XM_017009967.1:c.7013G>T	XP_016865456.1:p.Cys2338Phe
XM_017009968.2:c.7109G>T	XP_016865457.1:p.Cys2370Phe
XM_017009969.2:c.7109G>T	XP_016865458.1:p.Cys2370Phe
XM_017009970.2:c.7109G>T	XP_016865459.1:p.Cys2370Phe
XM_017009971.2:c.7109G>T	XP_016865460.1:p.Cys2370Phe
XM_017009972.1:c.227G>T	XP_016865461.1:p.Cys76Phe
XM_017009973.1:c.227G>T	XP_016865462.1:p.Cys76Phe
XM_017009974.2:c.7109G>T	XP_016865463.1:p.Cys2370Phe
NR_003149.2:n.7125G>T