Canonical Allele Identifier: CA360409056

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041476C>G (hg19) ; chr5:g.90745659C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745659C>G , CM000667.2:g.90745659C>G	GRCh38
NC_000005.9:g.90041476C>G , CM000667.1:g.90041476C>G	GRCh37
NC_000005.8:g.90077232C>G	NCBI36
NG_007083.1:g.191860C>G
NG_007083.2:g.221316C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10838C>G MANE Select	ENSP00000384582.2:p.Thr3613Arg
ENST00000639431.1:c.265+69450C>G	ENSP00000491057.1:n.265+69450C>G
ENST00000640374.1:n.3982C>G
ENST00000640464.1:n.1257C>G
ENST00000405460.6:c.10838C>G	ENSP00000384582.2:p.Thr3613Arg
ENST00000509621.1:c.3535C>G
NM_032119.3:c.10838C>G	NP_115495.3:p.Thr3613Arg
NR_003149.1:n.10851C>G
XM_011543675.1:c.10835C>G	XP_011541977.1:p.Thr3612Arg
XM_011543676.1:c.10757C>G	XP_011541978.1:p.Thr3586Arg
XM_011543677.1:c.8141C>G	XP_011541979.1:p.Thr2714Arg
XM_011543678.1:c.10838C>G	XP_011541980.1:p.Thr3613Arg
XM_011543679.1:c.*60C>G	XP_011541981.1:n.*60C>G
NM_032119.4:c.10838C>G MANE Select	NP_115495.3:p.Thr3613Arg
XM_017009963.2:c.10859C>G	XP_016865452.1:p.Thr3620Arg
XM_017009964.2:c.10856C>G	XP_016865453.1:p.Thr3619Arg
XM_017009965.1:c.10856C>G	XP_016865454.1:p.Thr3619Arg
XM_017009966.2:c.10778C>G	XP_016865455.1:p.Thr3593Arg
XM_017009967.1:c.10763C>G	XP_016865456.1:p.Thr3588Arg
XM_017009968.2:c.10859C>G	XP_016865457.1:p.Thr3620Arg
XM_017009969.2:c.10859C>G	XP_016865458.1:p.Thr3620Arg
XM_017009970.2:c.10859C>G	XP_016865459.1:p.Thr3620Arg
XM_017009971.2:c.10859C>G	XP_016865460.1:p.Thr3620Arg
XM_017009972.1:c.3977C>G	XP_016865461.1:p.Thr1326Arg
XM_017009973.1:c.3956C>G	XP_016865462.1:p.Thr1319Arg
XM_017009974.2:c.*60C>G	XP_016865463.1:n.*60C>G
NR_003149.2:n.10854C>G