Canonical Allele Identifier: CA360409127

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041492A>T (hg19) ; chr5:g.90745675A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745675A>T , CM000667.2:g.90745675A>T	GRCh38
NC_000005.9:g.90041492A>T , CM000667.1:g.90041492A>T	GRCh37
NC_000005.8:g.90077248A>T	NCBI36
NG_007083.1:g.191876A>T
NG_007083.2:g.221332A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10854A>T MANE Select	ENSP00000384582.2:p.Glu3618Asp
ENST00000639431.1:c.265+69466A>T	ENSP00000491057.1:n.265+69466A>T
ENST00000640374.1:n.3998A>T
ENST00000640464.1:n.1273A>T
ENST00000405460.6:c.10854A>T	ENSP00000384582.2:p.Glu3618Asp
ENST00000509621.1:c.3551A>T
NM_032119.3:c.10854A>T	NP_115495.3:p.Glu3618Asp
NR_003149.1:n.10867A>T
XM_011543675.1:c.10851A>T	XP_011541977.1:p.Glu3617Asp
XM_011543676.1:c.10773A>T	XP_011541978.1:p.Glu3591Asp
XM_011543677.1:c.8157A>T	XP_011541979.1:p.Glu2719Asp
XM_011543678.1:c.10854A>T	XP_011541980.1:p.Glu3618Asp
XM_011543679.1:c.*76A>T	XP_011541981.1:n.*76A>T
NM_032119.4:c.10854A>T MANE Select	NP_115495.3:p.Glu3618Asp
XM_017009963.2:c.10875A>T	XP_016865452.1:p.Glu3625Asp
XM_017009964.2:c.10872A>T	XP_016865453.1:p.Glu3624Asp
XM_017009965.1:c.10872A>T	XP_016865454.1:p.Glu3624Asp
XM_017009966.2:c.10794A>T	XP_016865455.1:p.Glu3598Asp
XM_017009967.1:c.10779A>T	XP_016865456.1:p.Glu3593Asp
XM_017009968.2:c.10875A>T	XP_016865457.1:p.Glu3625Asp
XM_017009969.2:c.10875A>T	XP_016865458.1:p.Glu3625Asp
XM_017009970.2:c.10875A>T	XP_016865459.1:p.Glu3625Asp
XM_017009971.2:c.10875A>T	XP_016865460.1:p.Glu3625Asp
XM_017009972.1:c.3993A>T	XP_016865461.1:p.Glu1331Asp
XM_017009973.1:c.3972A>T	XP_016865462.1:p.Glu1324Asp
XM_017009974.2:c.*76A>T	XP_016865463.1:n.*76A>T
NR_003149.2:n.10870A>T