Canonical Allele Identifier: CA360396207

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712329-A-T
• MyVariant Identifiers: chr5:g.90008146A>T (hg19) ; chr5:g.90712329A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712329A>T , CM000667.2:g.90712329A>T	GRCh38
NC_000005.9:g.90008146A>T , CM000667.1:g.90008146A>T	GRCh37
NC_000005.8:g.90043902A>T	NCBI36
NG_007083.1:g.158530A>T
NG_007083.2:g.187986A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9085A>T MANE Select	ENSP00000384582.2:p.Ile3029Phe
ENST00000639431.1:c.265+36120A>T	ENSP00000491057.1:n.265+36120A>T
ENST00000639473.1:n.4544A>T
ENST00000640012.1:c.2892A>T
ENST00000640374.1:n.2229A>T
ENST00000640779.1:c.3814A>T
ENST00000405460.6:c.9085A>T	ENSP00000384582.2:p.Ile3029Phe
ENST00000509621.1:c.1782A>T
NM_032119.3:c.9085A>T	NP_115495.3:p.Ile3029Phe
NR_003149.1:n.9098A>T
XM_011543675.1:c.9082A>T	XP_011541977.1:p.Ile3028Phe
XM_011543676.1:c.9004A>T	XP_011541978.1:p.Ile3002Phe
XM_011543677.1:c.6388A>T	XP_011541979.1:p.Ile2130Phe
XM_011543678.1:c.9085A>T	XP_011541980.1:p.Ile3029Phe
XM_011543679.1:c.9085A>T	XP_011541981.1:p.Ile3029Phe
NM_032119.4:c.9085A>T MANE Select	NP_115495.3:p.Ile3029Phe
XM_017009963.2:c.9106A>T	XP_016865452.1:p.Ile3036Phe
XM_017009964.2:c.9103A>T	XP_016865453.1:p.Ile3035Phe
XM_017009965.1:c.9103A>T	XP_016865454.1:p.Ile3035Phe
XM_017009966.2:c.9025A>T	XP_016865455.1:p.Ile3009Phe
XM_017009967.1:c.9010A>T	XP_016865456.1:p.Ile3004Phe
XM_017009968.2:c.9106A>T	XP_016865457.1:p.Ile3036Phe
XM_017009969.2:c.9106A>T	XP_016865458.1:p.Ile3036Phe
XM_017009970.2:c.9106A>T	XP_016865459.1:p.Ile3036Phe
XM_017009971.2:c.9106A>T	XP_016865460.1:p.Ile3036Phe
XM_017009972.1:c.2224A>T	XP_016865461.1:p.Ile742Phe
XM_017009973.1:c.2203A>T	XP_016865462.1:p.Ile735Phe
XM_017009974.2:c.9106A>T	XP_016865463.1:p.Ile3036Phe
NR_003149.2:n.9101A>T