Canonical Allele Identifier: CA360409684

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106553C>A (hg19) ; chr5:g.90810736C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810736C>A , CM000667.2:g.90810736C>A	GRCh38
NC_000005.9:g.90106553C>A , CM000667.1:g.90106553C>A	GRCh37
NC_000005.8:g.90142309C>A	NCBI36
NG_007083.1:g.256937C>A
NG_007083.2:g.286393C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.15476C>A MANE Select	ENSP00000384582.2:p.Thr5159Lys
ENST00000425867.3:c.4430C>A	ENSP00000392618.3:p.Thr1477Lys
ENST00000638510.1:n.2743C>A
ENST00000639431.1:c.265+134527C>A	ENSP00000491057.1:n.265+134527C>A
ENST00000640407.1:c.1886C>A	ENSP00000491425.1:p.Thr629Lys
ENST00000405460.6:c.15476C>A	ENSP00000384582.2:p.Thr5159Lys
ENST00000425867.2:c.2459C>A	ENSP00000392618.2:p.Thr820Lys
NM_032119.3:c.15476C>A	NP_115495.3:p.Thr5159Lys
NR_003149.1:n.15489C>A
XM_011543675.1:c.15473C>A	XP_011541977.1:p.Thr5158Lys
XM_011543676.1:c.15395C>A	XP_011541978.1:p.Thr5132Lys
XM_011543677.1:c.12779C>A	XP_011541979.1:p.Thr4260Lys
NM_032119.4:c.15476C>A MANE Select	NP_115495.3:p.Thr5159Lys
XM_017009963.2:c.15497C>A	XP_016865452.1:p.Thr5166Lys
XM_017009964.2:c.15494C>A	XP_016865453.1:p.Thr5165Lys
XM_017009965.1:c.15494C>A	XP_016865454.1:p.Thr5165Lys
XM_017009966.2:c.15416C>A	XP_016865455.1:p.Thr5139Lys
XM_017009967.1:c.15401C>A	XP_016865456.1:p.Thr5134Lys
XM_017009968.2:c.15317C>A	XP_016865457.1:p.Thr5106Lys
XM_017009969.2:c.15497C>A	XP_016865458.1:p.Thr5166Lys
XM_017009971.2:c.*430C>A	XP_016865460.1:n.*430C>A
XM_017009972.1:c.8615C>A	XP_016865461.1:p.Thr2872Lys
XM_017009973.1:c.8594C>A	XP_016865462.1:p.Thr2865Lys
NR_003149.2:n.15492C>A