Canonical Allele Identifier: CA445412046

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008211T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712394T>A , CM000667.2:g.90712394T>A	GRCh38
NC_000005.9:g.90008211T>A , CM000667.1:g.90008211T>A	GRCh37
NC_000005.8:g.90043967T>A	NCBI36
NG_007083.1:g.158595T>A
NG_007083.2:g.188051T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9150T>A MANE Select	ENSP00000384582.2:p.Pro3050=
ENST00000639431.1:c.265+36185T>A	ENSP00000491057.1:n.265+36185T>A
ENST00000639473.1:n.4609T>A
ENST00000640012.1:c.2957T>A
ENST00000640374.1:n.2294T>A
ENST00000640779.1:c.3879T>A
ENST00000405460.6:c.9150T>A	ENSP00000384582.2:p.Pro3050=
ENST00000509621.1:c.1847T>A
NM_032119.3:c.9150T>A	NP_115495.3:p.Pro3050=
NR_003149.1:n.9163T>A
XM_011543675.1:c.9147T>A	XP_011541977.1:p.Pro3049=
XM_011543676.1:c.9069T>A	XP_011541978.1:p.Pro3023=
XM_011543677.1:c.6453T>A	XP_011541979.1:p.Pro2151=
XM_011543678.1:c.9150T>A	XP_011541980.1:p.Pro3050=
XM_011543679.1:c.9150T>A	XP_011541981.1:p.Pro3050=
XR_948560.1:n.452A>T
NM_032119.4:c.9150T>A MANE Select	NP_115495.3:p.Pro3050=
XM_017009963.2:c.9171T>A	XP_016865452.1:p.Pro3057=
XM_017009964.2:c.9168T>A	XP_016865453.1:p.Pro3056=
XM_017009965.1:c.9168T>A	XP_016865454.1:p.Pro3056=
XM_017009966.2:c.9090T>A	XP_016865455.1:p.Pro3030=
XM_017009967.1:c.9075T>A	XP_016865456.1:p.Pro3025=
XM_017009968.2:c.9171T>A	XP_016865457.1:p.Pro3057=
XM_017009969.2:c.9171T>A	XP_016865458.1:p.Pro3057=
XM_017009970.2:c.9171T>A	XP_016865459.1:p.Pro3057=
XM_017009971.2:c.9171T>A	XP_016865460.1:p.Pro3057=
XM_017009972.1:c.2289T>A	XP_016865461.1:p.Pro763=
XM_017009973.1:c.2268T>A	XP_016865462.1:p.Pro756=
XM_017009974.2:c.9171T>A	XP_016865463.1:p.Pro3057=
NR_003149.2:n.9166T>A