Canonical Allele Identifier: CA360398870

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90085591G>T (hg19) ; chr5:g.90789774G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789774G>T , CM000667.2:g.90789774G>T	GRCh38
NC_000005.9:g.90085591G>T , CM000667.1:g.90085591G>T	GRCh37
NC_000005.8:g.90121347G>T	NCBI36
NG_007083.1:g.235975G>T
NG_007083.2:g.265431G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.13966G>T MANE Select	ENSP00000384582.2:p.Glu4656Ter
ENST00000425867.3:c.2920G>T	ENSP00000392618.3:p.Glu974Ter
ENST00000638510.1:n.1233G>T
ENST00000638975.1:c.595G>T	ENSP00000492630.1:p.Glu199Ter
ENST00000639431.1:c.265+113565G>T	ENSP00000491057.1:n.265+113565G>T
ENST00000640407.1:c.376G>T	ENSP00000491425.1:p.Glu126Ter
ENST00000405460.6:c.13966G>T	ENSP00000384582.2:p.Glu4656Ter
ENST00000425867.2:c.949G>T	ENSP00000392618.2:p.Glu317Ter
NM_032119.3:c.13966G>T	NP_115495.3:p.Glu4656Ter
NR_003149.1:n.13979G>T
XM_011543675.1:c.13963G>T	XP_011541977.1:p.Glu4655Ter
XM_011543676.1:c.13885G>T	XP_011541978.1:p.Glu4629Ter
XM_011543677.1:c.11269G>T	XP_011541979.1:p.Glu3757Ter
XM_011543678.1:c.13966G>T	XP_011541980.1:p.Glu4656Ter
NM_032119.4:c.13966G>T MANE Select	NP_115495.3:p.Glu4656Ter
XM_017009963.2:c.13987G>T	XP_016865452.1:p.Glu4663Ter
XM_017009964.2:c.13984G>T	XP_016865453.1:p.Glu4662Ter
XM_017009965.1:c.13984G>T	XP_016865454.1:p.Glu4662Ter
XM_017009966.2:c.13906G>T	XP_016865455.1:p.Glu4636Ter
XM_017009967.1:c.13891G>T	XP_016865456.1:p.Glu4631Ter
XM_017009968.2:c.13987G>T	XP_016865457.1:p.Glu4663Ter
XM_017009969.2:c.13987G>T	XP_016865458.1:p.Glu4663Ter
XM_017009970.2:c.13987G>T	XP_016865459.1:p.Glu4663Ter
XM_017009971.2:c.13987G>T	XP_016865460.1:p.Glu4663Ter
XM_017009972.1:c.7105G>T	XP_016865461.1:p.Glu2369Ter
XM_017009973.1:c.7084G>T	XP_016865462.1:p.Glu2362Ter
NR_003149.2:n.13982G>T