Canonical Allele Identifier: CA360396113

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008104A>T (hg19) ; chr5:g.90712287A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712287A>T , CM000667.2:g.90712287A>T	GRCh38
NC_000005.9:g.90008104A>T , CM000667.1:g.90008104A>T	GRCh37
NC_000005.8:g.90043860A>T	NCBI36
NG_007083.1:g.158488A>T
NG_007083.2:g.187944A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9043A>T MANE Select	ENSP00000384582.2:p.Ile3015Phe
ENST00000639431.1:c.265+36078A>T	ENSP00000491057.1:n.265+36078A>T
ENST00000639473.1:n.4502A>T
ENST00000640012.1:c.2850A>T
ENST00000640374.1:n.2187A>T
ENST00000640779.1:c.3772A>T
ENST00000405460.6:c.9043A>T	ENSP00000384582.2:p.Ile3015Phe
ENST00000509621.1:c.1740A>T
NM_032119.3:c.9043A>T	NP_115495.3:p.Ile3015Phe
NR_003149.1:n.9056A>T
XM_011543675.1:c.9040A>T	XP_011541977.1:p.Ile3014Phe
XM_011543676.1:c.8962A>T	XP_011541978.1:p.Ile2988Phe
XM_011543677.1:c.6346A>T	XP_011541979.1:p.Ile2116Phe
XM_011543678.1:c.9043A>T	XP_011541980.1:p.Ile3015Phe
XM_011543679.1:c.9043A>T	XP_011541981.1:p.Ile3015Phe
NM_032119.4:c.9043A>T MANE Select	NP_115495.3:p.Ile3015Phe
XM_017009963.2:c.9064A>T	XP_016865452.1:p.Ile3022Phe
XM_017009964.2:c.9061A>T	XP_016865453.1:p.Ile3021Phe
XM_017009965.1:c.9061A>T	XP_016865454.1:p.Ile3021Phe
XM_017009966.2:c.8983A>T	XP_016865455.1:p.Ile2995Phe
XM_017009967.1:c.8968A>T	XP_016865456.1:p.Ile2990Phe
XM_017009968.2:c.9064A>T	XP_016865457.1:p.Ile3022Phe
XM_017009969.2:c.9064A>T	XP_016865458.1:p.Ile3022Phe
XM_017009970.2:c.9064A>T	XP_016865459.1:p.Ile3022Phe
XM_017009971.2:c.9064A>T	XP_016865460.1:p.Ile3022Phe
XM_017009972.1:c.2182A>T	XP_016865461.1:p.Ile728Phe
XM_017009973.1:c.2161A>T	XP_016865462.1:p.Ile721Phe
XM_017009974.2:c.9064A>T	XP_016865463.1:p.Ile3022Phe
NR_003149.2:n.9059A>T