Canonical Allele Identifier: CA360397535

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012463A>G (hg19) ; chr5:g.90716646A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716646A>G , CM000667.2:g.90716646A>G	GRCh38
NC_000005.9:g.90012463A>G , CM000667.1:g.90012463A>G	GRCh37
NC_000005.8:g.90048219A>G	NCBI36
NG_007083.1:g.162847A>G
NG_007083.2:g.192303A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9364A>G MANE Select	ENSP00000384582.2:p.Thr3122Ala
ENST00000639431.1:c.265+40437A>G	ENSP00000491057.1:n.265+40437A>G
ENST00000639473.1:n.4823A>G
ENST00000640012.1:c.3171A>G
ENST00000640374.1:n.2508A>G
ENST00000640779.1:c.4093A>G
ENST00000405460.6:c.9364A>G	ENSP00000384582.2:p.Thr3122Ala
ENST00000509621.1:c.2061A>G
NM_032119.3:c.9364A>G	NP_115495.3:p.Thr3122Ala
NR_003149.1:n.9377A>G
XM_011543675.1:c.9361A>G	XP_011541977.1:p.Thr3121Ala
XM_011543676.1:c.9283A>G	XP_011541978.1:p.Thr3095Ala
XM_011543677.1:c.6667A>G	XP_011541979.1:p.Thr2223Ala
XM_011543678.1:c.9364A>G	XP_011541980.1:p.Thr3122Ala
XM_011543679.1:c.9364A>G	XP_011541981.1:p.Thr3122Ala
XR_948560.1:n.272-837T>C
NM_032119.4:c.9364A>G MANE Select	NP_115495.3:p.Thr3122Ala
XM_017009963.2:c.9385A>G	XP_016865452.1:p.Thr3129Ala
XM_017009964.2:c.9382A>G	XP_016865453.1:p.Thr3128Ala
XM_017009965.1:c.9382A>G	XP_016865454.1:p.Thr3128Ala
XM_017009966.2:c.9304A>G	XP_016865455.1:p.Thr3102Ala
XM_017009967.1:c.9289A>G	XP_016865456.1:p.Thr3097Ala
XM_017009968.2:c.9385A>G	XP_016865457.1:p.Thr3129Ala
XM_017009969.2:c.9385A>G	XP_016865458.1:p.Thr3129Ala
XM_017009970.2:c.9385A>G	XP_016865459.1:p.Thr3129Ala
XM_017009971.2:c.9385A>G	XP_016865460.1:p.Thr3129Ala
XM_017009972.1:c.2503A>G	XP_016865461.1:p.Thr835Ala
XM_017009973.1:c.2482A>G	XP_016865462.1:p.Thr828Ala
XM_017009974.2:c.9385A>G	XP_016865463.1:p.Thr3129Ala
XR_001742802.1:n.2523-837T>C
NR_003149.2:n.9380A>G