Canonical Allele Identifier: CA445436561

Gene: ADGRV1

Linked Data

• dbSNP Id: rs939209600
• MyVariant Identifiers: chr5:g.90119314G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823497G>T , CM000667.2:g.90823497G>T	GRCh38
NC_000005.9:g.90119314G>T , CM000667.1:g.90119314G>T	GRCh37
NC_000005.8:g.90155070G>T	NCBI36
NG_007083.1:g.269698G>T
NG_007083.2:g.299154G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16269G>T MANE Select	ENSP00000384582.2:p.Gly5423=
ENST00000425867.3:c.5223G>T	ENSP00000392618.3:p.Gly1741=
ENST00000638510.1:n.3536G>T
ENST00000639431.1:c.265+147288G>T	ENSP00000491057.1:n.265+147288G>T
ENST00000640061.1:n.128+1315G>T
ENST00000640407.1:c.2679G>T	ENSP00000491425.1:p.Gly893=
ENST00000405460.6:c.16269G>T	ENSP00000384582.2:p.Gly5423=
ENST00000425867.2:c.3252G>T	ENSP00000392618.2:p.Gly1084=
NM_032119.3:c.16269G>T	NP_115495.3:p.Gly5423=
NR_003149.1:n.16282G>T
XM_011543675.1:c.16266G>T	XP_011541977.1:p.Gly5422=
XM_011543676.1:c.16188G>T	XP_011541978.1:p.Gly5396=
XM_011543677.1:c.13572G>T	XP_011541979.1:p.Gly4524=
NM_032119.4:c.16269G>T MANE Select	NP_115495.3:p.Gly5423=
XM_017009963.2:c.16290G>T	XP_016865452.1:p.Gly5430=
XM_017009964.2:c.16287G>T	XP_016865453.1:p.Gly5429=
XM_017009965.1:c.16287G>T	XP_016865454.1:p.Gly5429=
XM_017009966.2:c.16209G>T	XP_016865455.1:p.Gly5403=
XM_017009967.1:c.16194G>T	XP_016865456.1:p.Gly5398=
XM_017009968.2:c.16110G>T	XP_016865457.1:p.Gly5370=
XM_017009969.2:c.16290G>T	XP_016865458.1:p.Gly5430=
XM_017009972.1:c.9408G>T	XP_016865461.1:p.Gly3136=
XM_017009973.1:c.9387G>T	XP_016865462.1:p.Gly3129=
NR_003149.2:n.16285G>T