Canonical Allele Identifier: CA445414796

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90021398A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725581A>G , CM000667.2:g.90725581A>G	GRCh38
NC_000005.9:g.90021398A>G , CM000667.1:g.90021398A>G	GRCh37
NC_000005.8:g.90057154A>G	NCBI36
NG_007083.1:g.171782A>G
NG_007083.2:g.201238A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10086A>G MANE Select	ENSP00000384582.2:p.Gln3362=
ENST00000639431.1:c.265+49372A>G	ENSP00000491057.1:n.265+49372A>G
ENST00000640374.1:n.3230A>G
ENST00000640464.1:n.505A>G
ENST00000405460.6:c.10086A>G	ENSP00000384582.2:p.Gln3362=
ENST00000509621.1:c.2783A>G
NM_032119.3:c.10086A>G	NP_115495.3:p.Gln3362=
NR_003149.1:n.10099A>G
XM_011543675.1:c.10083A>G	XP_011541977.1:p.Gln3361=
XM_011543676.1:c.10005A>G	XP_011541978.1:p.Gln3335=
XM_011543677.1:c.7389A>G	XP_011541979.1:p.Gln2463=
XM_011543678.1:c.10086A>G	XP_011541980.1:p.Gln3362=
XM_011543679.1:c.10086A>G	XP_011541981.1:p.Gln3362=
XR_948560.1:n.272-9772T>C
NM_032119.4:c.10086A>G MANE Select	NP_115495.3:p.Gln3362=
XM_017009963.2:c.10107A>G	XP_016865452.1:p.Gln3369=
XM_017009964.2:c.10104A>G	XP_016865453.1:p.Gln3368=
XM_017009965.1:c.10104A>G	XP_016865454.1:p.Gln3368=
XM_017009966.2:c.10026A>G	XP_016865455.1:p.Gln3342=
XM_017009967.1:c.10011A>G	XP_016865456.1:p.Gln3337=
XM_017009968.2:c.10107A>G	XP_016865457.1:p.Gln3369=
XM_017009969.2:c.10107A>G	XP_016865458.1:p.Gln3369=
XM_017009970.2:c.10107A>G	XP_016865459.1:p.Gln3369=
XM_017009971.2:c.10107A>G	XP_016865460.1:p.Gln3369=
XM_017009972.1:c.3225A>G	XP_016865461.1:p.Gln1075=
XM_017009973.1:c.3204A>G	XP_016865462.1:p.Gln1068=
XM_017009974.2:c.10107A>G	XP_016865463.1:p.Gln3369=
XR_001742802.1:n.2523-9772T>C
NR_003149.2:n.10102A>G