Canonical Allele Identifier: CA360396194

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008140G>T (hg19) ; chr5:g.90712323G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712323G>T , CM000667.2:g.90712323G>T	GRCh38
NC_000005.9:g.90008140G>T , CM000667.1:g.90008140G>T	GRCh37
NC_000005.8:g.90043896G>T	NCBI36
NG_007083.1:g.158524G>T
NG_007083.2:g.187980G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9079G>T MANE Select	ENSP00000384582.2:p.Val3027Phe
ENST00000639431.1:c.265+36114G>T	ENSP00000491057.1:n.265+36114G>T
ENST00000639473.1:n.4538G>T
ENST00000640012.1:c.2886G>T
ENST00000640374.1:n.2223G>T
ENST00000640779.1:c.3808G>T
ENST00000405460.6:c.9079G>T	ENSP00000384582.2:p.Val3027Phe
ENST00000509621.1:c.1776G>T
NM_032119.3:c.9079G>T	NP_115495.3:p.Val3027Phe
NR_003149.1:n.9092G>T
XM_011543675.1:c.9076G>T	XP_011541977.1:p.Val3026Phe
XM_011543676.1:c.8998G>T	XP_011541978.1:p.Val3000Phe
XM_011543677.1:c.6382G>T	XP_011541979.1:p.Val2128Phe
XM_011543678.1:c.9079G>T	XP_011541980.1:p.Val3027Phe
XM_011543679.1:c.9079G>T	XP_011541981.1:p.Val3027Phe
NM_032119.4:c.9079G>T MANE Select	NP_115495.3:p.Val3027Phe
XM_017009963.2:c.9100G>T	XP_016865452.1:p.Val3034Phe
XM_017009964.2:c.9097G>T	XP_016865453.1:p.Val3033Phe
XM_017009965.1:c.9097G>T	XP_016865454.1:p.Val3033Phe
XM_017009966.2:c.9019G>T	XP_016865455.1:p.Val3007Phe
XM_017009967.1:c.9004G>T	XP_016865456.1:p.Val3002Phe
XM_017009968.2:c.9100G>T	XP_016865457.1:p.Val3034Phe
XM_017009969.2:c.9100G>T	XP_016865458.1:p.Val3034Phe
XM_017009970.2:c.9100G>T	XP_016865459.1:p.Val3034Phe
XM_017009971.2:c.9100G>T	XP_016865460.1:p.Val3034Phe
XM_017009972.1:c.2218G>T	XP_016865461.1:p.Val740Phe
XM_017009973.1:c.2197G>T	XP_016865462.1:p.Val733Phe
XM_017009974.2:c.9100G>T	XP_016865463.1:p.Val3034Phe
NR_003149.2:n.9095G>T