Canonical Allele Identifier: CA445411845

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008148C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712331C>T , CM000667.2:g.90712331C>T	GRCh38
NC_000005.9:g.90008148C>T , CM000667.1:g.90008148C>T	GRCh37
NC_000005.8:g.90043904C>T	NCBI36
NG_007083.1:g.158532C>T
NG_007083.2:g.187988C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9087C>T MANE Select	ENSP00000384582.2:p.Ile3029=
ENST00000639431.1:c.265+36122C>T	ENSP00000491057.1:n.265+36122C>T
ENST00000639473.1:n.4546C>T
ENST00000640012.1:c.2894C>T
ENST00000640374.1:n.2231C>T
ENST00000640779.1:c.3816C>T
ENST00000405460.6:c.9087C>T	ENSP00000384582.2:p.Ile3029=
ENST00000509621.1:c.1784C>T
NM_032119.3:c.9087C>T	NP_115495.3:p.Ile3029=
NR_003149.1:n.9100C>T
XM_011543675.1:c.9084C>T	XP_011541977.1:p.Ile3028=
XM_011543676.1:c.9006C>T	XP_011541978.1:p.Ile3002=
XM_011543677.1:c.6390C>T	XP_011541979.1:p.Ile2130=
XM_011543678.1:c.9087C>T	XP_011541980.1:p.Ile3029=
XM_011543679.1:c.9087C>T	XP_011541981.1:p.Ile3029=
NM_032119.4:c.9087C>T MANE Select	NP_115495.3:p.Ile3029=
XM_017009963.2:c.9108C>T	XP_016865452.1:p.Ile3036=
XM_017009964.2:c.9105C>T	XP_016865453.1:p.Ile3035=
XM_017009965.1:c.9105C>T	XP_016865454.1:p.Ile3035=
XM_017009966.2:c.9027C>T	XP_016865455.1:p.Ile3009=
XM_017009967.1:c.9012C>T	XP_016865456.1:p.Ile3004=
XM_017009968.2:c.9108C>T	XP_016865457.1:p.Ile3036=
XM_017009969.2:c.9108C>T	XP_016865458.1:p.Ile3036=
XM_017009970.2:c.9108C>T	XP_016865459.1:p.Ile3036=
XM_017009971.2:c.9108C>T	XP_016865460.1:p.Ile3036=
XM_017009972.1:c.2226C>T	XP_016865461.1:p.Ile742=
XM_017009973.1:c.2205C>T	XP_016865462.1:p.Ile735=
XM_017009974.2:c.9108C>T	XP_016865463.1:p.Ile3036=
NR_003149.2:n.9103C>T