Canonical Allele Identifier: CA360410705

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106819A>G (hg19) ; chr5:g.90811002A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811002A>G , CM000667.2:g.90811002A>G	GRCh38
NC_000005.9:g.90106819A>G , CM000667.1:g.90106819A>G	GRCh37
NC_000005.8:g.90142575A>G	NCBI36
NG_007083.1:g.257203A>G
NG_007083.2:g.286659A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15742A>G MANE Select	ENSP00000384582.2:p.Thr5248Ala
ENST00000425867.3:c.4696A>G	ENSP00000392618.3:p.Thr1566Ala
ENST00000638510.1:n.3009A>G
ENST00000639431.1:c.265+134793A>G	ENSP00000491057.1:n.265+134793A>G
ENST00000640407.1:c.2152A>G	ENSP00000491425.1:p.Thr718Ala
ENST00000405460.6:c.15742A>G	ENSP00000384582.2:p.Thr5248Ala
ENST00000425867.2:c.2725A>G	ENSP00000392618.2:p.Thr909Ala
NM_032119.3:c.15742A>G	NP_115495.3:p.Thr5248Ala
NR_003149.1:n.15755A>G
XM_011543675.1:c.15739A>G	XP_011541977.1:p.Thr5247Ala
XM_011543676.1:c.15661A>G	XP_011541978.1:p.Thr5221Ala
XM_011543677.1:c.13045A>G	XP_011541979.1:p.Thr4349Ala
NM_032119.4:c.15742A>G MANE Select	NP_115495.3:p.Thr5248Ala
XM_017009963.2:c.15763A>G	XP_016865452.1:p.Thr5255Ala
XM_017009964.2:c.15760A>G	XP_016865453.1:p.Thr5254Ala
XM_017009965.1:c.15760A>G	XP_016865454.1:p.Thr5254Ala
XM_017009966.2:c.15682A>G	XP_016865455.1:p.Thr5228Ala
XM_017009967.1:c.15667A>G	XP_016865456.1:p.Thr5223Ala
XM_017009968.2:c.15583A>G	XP_016865457.1:p.Thr5195Ala
XM_017009969.2:c.15763A>G	XP_016865458.1:p.Thr5255Ala
XM_017009972.1:c.8881A>G	XP_016865461.1:p.Thr2961Ala
XM_017009973.1:c.8860A>G	XP_016865462.1:p.Thr2954Ala
NR_003149.2:n.15758A>G