Canonical Allele Identifier: CA360425780

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119408G>T (hg19) ; chr5:g.90823591G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823591G>T , CM000667.2:g.90823591G>T	GRCh38
NC_000005.9:g.90119408G>T , CM000667.1:g.90119408G>T	GRCh37
NC_000005.8:g.90155164G>T	NCBI36
NG_007083.1:g.269792G>T
NG_007083.2:g.299248G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16363G>T MANE Select	ENSP00000384582.2:p.Glu5455Ter
ENST00000425867.3:c.5317G>T	ENSP00000392618.3:p.Glu1773Ter
ENST00000638510.1:n.3630G>T
ENST00000639431.1:c.265+147382G>T	ENSP00000491057.1:n.265+147382G>T
ENST00000640061.1:n.128+1409G>T
ENST00000640407.1:c.2773G>T	ENSP00000491425.1:p.Glu925Ter
ENST00000405460.6:c.16363G>T	ENSP00000384582.2:p.Glu5455Ter
ENST00000425867.2:c.3346G>T	ENSP00000392618.2:p.Glu1116Ter
NM_032119.3:c.16363G>T	NP_115495.3:p.Glu5455Ter
NR_003149.1:n.16376G>T
XM_011543675.1:c.16360G>T	XP_011541977.1:p.Glu5454Ter
XM_011543676.1:c.16282G>T	XP_011541978.1:p.Glu5428Ter
XM_011543677.1:c.13666G>T	XP_011541979.1:p.Glu4556Ter
NM_032119.4:c.16363G>T MANE Select	NP_115495.3:p.Glu5455Ter
XM_017009963.2:c.16384G>T	XP_016865452.1:p.Glu5462Ter
XM_017009964.2:c.16381G>T	XP_016865453.1:p.Glu5461Ter
XM_017009965.1:c.16381G>T	XP_016865454.1:p.Glu5461Ter
XM_017009966.2:c.16303G>T	XP_016865455.1:p.Glu5435Ter
XM_017009967.1:c.16288G>T	XP_016865456.1:p.Glu5430Ter
XM_017009968.2:c.16204G>T	XP_016865457.1:p.Glu5402Ter
XM_017009969.2:c.16384G>T	XP_016865458.1:p.Glu5462Ter
XM_017009972.1:c.9502G>T	XP_016865461.1:p.Glu3168Ter
XM_017009973.1:c.9481G>T	XP_016865462.1:p.Glu3161Ter
NR_003149.2:n.16379G>T