Canonical Allele Identifier: CA3338429

Gene: ADGRV1

Linked Data

• dbSNP Id: rs753583712
• ExAC: 5:89913701 G / T
• gnomAD v2: 5-89913701-G-T
• gnomAD v3: 5-90617884-G-T
• gnomAD v4: 5-90617884-G-T
• MyVariant Identifiers: chr5:g.89913701G>T (hg19) ; chr5:g.90617884G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617884G>T , CM000667.2:g.90617884G>T	GRCh38
NC_000005.9:g.89913701G>T , CM000667.1:g.89913701G>T	GRCh37
NC_000005.8:g.89949457G>T	NCBI36
NG_007083.1:g.64085G>T
NG_007083.2:g.93541G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.288G>T MANE Select	ENSP00000384582.2:p.Val96=
ENST00000638316.1:n.498G>T
ENST00000638638.1:n.695G>T
ENST00000640109.1:n.384G>T
ENST00000640281.1:n.347G>T
ENST00000405460.6:c.288G>T	ENSP00000384582.2:p.Val96=
ENST00000508842.5:c.300G>T	ENSP00000425936.1:p.Val100=
NM_032119.3:c.288G>T	NP_115495.3:p.Val96=
NR_003149.1:n.384G>T
XM_011543675.1:c.288G>T	XP_011541977.1:p.Val96=
XM_011543676.1:c.288G>T	XP_011541978.1:p.Val96=
XM_011543678.1:c.288G>T	XP_011541980.1:p.Val96=
XM_011543679.1:c.288G>T	XP_011541981.1:p.Val96=
NM_032119.4:c.288G>T MANE Select	NP_115495.3:p.Val96=
XM_017009963.2:c.288G>T	XP_016865452.1:p.Val96=
XM_017009964.2:c.288G>T	XP_016865453.1:p.Val96=
XM_017009965.1:c.285G>T	XP_016865454.1:p.Val95=
XM_017009966.2:c.288G>T	XP_016865455.1:p.Val96=
XM_017009967.1:c.288G>T	XP_016865456.1:p.Val96=
XM_017009968.2:c.288G>T	XP_016865457.1:p.Val96=
XM_017009969.2:c.288G>T	XP_016865458.1:p.Val96=
XM_017009970.2:c.288G>T	XP_016865459.1:p.Val96=
XM_017009971.2:c.288G>T	XP_016865460.1:p.Val96=
XM_017009974.2:c.288G>T	XP_016865463.1:p.Val96=
NR_003149.2:n.387G>T