Canonical Allele Identifier: CA445413810

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012471G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716654G>T , CM000667.2:g.90716654G>T	GRCh38
NC_000005.9:g.90012471G>T , CM000667.1:g.90012471G>T	GRCh37
NC_000005.8:g.90048227G>T	NCBI36
NG_007083.1:g.162855G>T
NG_007083.2:g.192311G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9372G>T MANE Select	ENSP00000384582.2:p.Val3124=
ENST00000639431.1:c.265+40445G>T	ENSP00000491057.1:n.265+40445G>T
ENST00000639473.1:n.4831G>T
ENST00000640012.1:c.3179G>T
ENST00000640374.1:n.2516G>T
ENST00000640779.1:c.4101G>T
ENST00000405460.6:c.9372G>T	ENSP00000384582.2:p.Val3124=
ENST00000509621.1:c.2069G>T
NM_032119.3:c.9372G>T	NP_115495.3:p.Val3124=
NR_003149.1:n.9385G>T
XM_011543675.1:c.9369G>T	XP_011541977.1:p.Val3123=
XM_011543676.1:c.9291G>T	XP_011541978.1:p.Val3097=
XM_011543677.1:c.6675G>T	XP_011541979.1:p.Val2225=
XM_011543678.1:c.9372G>T	XP_011541980.1:p.Val3124=
XM_011543679.1:c.9372G>T	XP_011541981.1:p.Val3124=
XR_948560.1:n.272-845C>A
NM_032119.4:c.9372G>T MANE Select	NP_115495.3:p.Val3124=
XM_017009963.2:c.9393G>T	XP_016865452.1:p.Val3131=
XM_017009964.2:c.9390G>T	XP_016865453.1:p.Val3130=
XM_017009965.1:c.9390G>T	XP_016865454.1:p.Val3130=
XM_017009966.2:c.9312G>T	XP_016865455.1:p.Val3104=
XM_017009967.1:c.9297G>T	XP_016865456.1:p.Val3099=
XM_017009968.2:c.9393G>T	XP_016865457.1:p.Val3131=
XM_017009969.2:c.9393G>T	XP_016865458.1:p.Val3131=
XM_017009970.2:c.9393G>T	XP_016865459.1:p.Val3131=
XM_017009971.2:c.9393G>T	XP_016865460.1:p.Val3131=
XM_017009972.1:c.2511G>T	XP_016865461.1:p.Val837=
XM_017009973.1:c.2490G>T	XP_016865462.1:p.Val830=
XM_017009974.2:c.9393G>T	XP_016865463.1:p.Val3131=
XR_001742802.1:n.2523-845C>A
NR_003149.2:n.9388G>T