Canonical Allele Identifier: CA360397838

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90716730-G-T
• MyVariant Identifiers: chr5:g.90012547G>T (hg19) ; chr5:g.90716730G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716730G>T , CM000667.2:g.90716730G>T	GRCh38
NC_000005.9:g.90012547G>T , CM000667.1:g.90012547G>T	GRCh37
NC_000005.8:g.90048303G>T	NCBI36
NG_007083.1:g.162931G>T
NG_007083.2:g.192387G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9447+1G>T MANE Select	ENSP00000384582.2:n.9447+1G>T
ENST00000639431.1:c.265+40521G>T	ENSP00000491057.1:n.265+40521G>T
ENST00000639473.1:n.4907G>T
ENST00000640374.1:n.2591+1G>T
ENST00000640779.1:c.4176+1G>T
ENST00000405460.6:c.9447+1G>T	ENSP00000384582.2:n.9447+1G>T
ENST00000509621.1:c.2144+1G>T
NM_032119.3:c.9447+1G>T	NP_115495.3:n.9447+1G>T
NR_003149.1:n.9460+1G>T
XM_011543675.1:c.9444+1G>T	XP_011541977.1:n.9444+1G>T
XM_011543676.1:c.9366+1G>T	XP_011541978.1:n.9366+1G>T
XM_011543677.1:c.6750+1G>T	XP_011541979.1:n.6750+1G>T
XM_011543678.1:c.9447+1G>T	XP_011541980.1:n.9447+1G>T
XM_011543679.1:c.9447+1G>T	XP_011541981.1:n.9447+1G>T
XR_948560.1:n.272-921C>A
NM_032119.4:c.9447+1G>T MANE Select	NP_115495.3:n.9447+1G>T
XM_017009963.2:c.9468+1G>T	XP_016865452.1:n.9468+1G>T
XM_017009964.2:c.9465+1G>T	XP_016865453.1:n.9465+1G>T
XM_017009965.1:c.9465+1G>T	XP_016865454.1:n.9465+1G>T
XM_017009966.2:c.9387+1G>T	XP_016865455.1:n.9387+1G>T
XM_017009967.1:c.9372+1G>T	XP_016865456.1:n.9372+1G>T
XM_017009968.2:c.9468+1G>T	XP_016865457.1:n.9468+1G>T
XM_017009969.2:c.9468+1G>T	XP_016865458.1:n.9468+1G>T
XM_017009970.2:c.9468+1G>T	XP_016865459.1:n.9468+1G>T
XM_017009971.2:c.9468+1G>T	XP_016865460.1:n.9468+1G>T
XM_017009972.1:c.2586+1G>T	XP_016865461.1:n.2586+1G>T
XM_017009973.1:c.2565+1G>T	XP_016865462.1:n.2565+1G>T
XM_017009974.2:c.9468+1G>T	XP_016865463.1:n.9468+1G>T
XR_001742802.1:n.2523-921C>A
NR_003149.2:n.9463+1G>T