Canonical Allele Identifier: CA360396152

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008122G>T (hg19) ; chr5:g.90712305G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712305G>T , CM000667.2:g.90712305G>T	GRCh38
NC_000005.9:g.90008122G>T , CM000667.1:g.90008122G>T	GRCh37
NC_000005.8:g.90043878G>T	NCBI36
NG_007083.1:g.158506G>T
NG_007083.2:g.187962G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9061G>T MANE Select	ENSP00000384582.2:p.Gly3021Ter
ENST00000639431.1:c.265+36096G>T	ENSP00000491057.1:n.265+36096G>T
ENST00000639473.1:n.4520G>T
ENST00000640012.1:c.2868G>T
ENST00000640374.1:n.2205G>T
ENST00000640779.1:c.3790G>T
ENST00000405460.6:c.9061G>T	ENSP00000384582.2:p.Gly3021Ter
ENST00000509621.1:c.1758G>T
NM_032119.3:c.9061G>T	NP_115495.3:p.Gly3021Ter
NR_003149.1:n.9074G>T
XM_011543675.1:c.9058G>T	XP_011541977.1:p.Gly3020Ter
XM_011543676.1:c.8980G>T	XP_011541978.1:p.Gly2994Ter
XM_011543677.1:c.6364G>T	XP_011541979.1:p.Gly2122Ter
XM_011543678.1:c.9061G>T	XP_011541980.1:p.Gly3021Ter
XM_011543679.1:c.9061G>T	XP_011541981.1:p.Gly3021Ter
NM_032119.4:c.9061G>T MANE Select	NP_115495.3:p.Gly3021Ter
XM_017009963.2:c.9082G>T	XP_016865452.1:p.Gly3028Ter
XM_017009964.2:c.9079G>T	XP_016865453.1:p.Gly3027Ter
XM_017009965.1:c.9079G>T	XP_016865454.1:p.Gly3027Ter
XM_017009966.2:c.9001G>T	XP_016865455.1:p.Gly3001Ter
XM_017009967.1:c.8986G>T	XP_016865456.1:p.Gly2996Ter
XM_017009968.2:c.9082G>T	XP_016865457.1:p.Gly3028Ter
XM_017009969.2:c.9082G>T	XP_016865458.1:p.Gly3028Ter
XM_017009970.2:c.9082G>T	XP_016865459.1:p.Gly3028Ter
XM_017009971.2:c.9082G>T	XP_016865460.1:p.Gly3028Ter
XM_017009972.1:c.2200G>T	XP_016865461.1:p.Gly734Ter
XM_017009973.1:c.2179G>T	XP_016865462.1:p.Gly727Ter
XM_017009974.2:c.9082G>T	XP_016865463.1:p.Gly3028Ter
NR_003149.2:n.9077G>T