Canonical Allele Identifier: CA360425583

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90823496-G-T
• MyVariant Identifiers: chr5:g.90119313G>T (hg19) ; chr5:g.90823496G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823496G>T , CM000667.2:g.90823496G>T	GRCh38
NC_000005.9:g.90119313G>T , CM000667.1:g.90119313G>T	GRCh37
NC_000005.8:g.90155069G>T	NCBI36
NG_007083.1:g.269697G>T
NG_007083.2:g.299153G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16268G>T MANE Select	ENSP00000384582.2:p.Gly5423Val
ENST00000425867.3:c.5222G>T	ENSP00000392618.3:p.Gly1741Val
ENST00000638510.1:n.3535G>T
ENST00000639431.1:c.265+147287G>T	ENSP00000491057.1:n.265+147287G>T
ENST00000640061.1:n.128+1314G>T
ENST00000640407.1:c.2678G>T	ENSP00000491425.1:p.Gly893Val
ENST00000405460.6:c.16268G>T	ENSP00000384582.2:p.Gly5423Val
ENST00000425867.2:c.3251G>T	ENSP00000392618.2:p.Gly1084Val
NM_032119.3:c.16268G>T	NP_115495.3:p.Gly5423Val
NR_003149.1:n.16281G>T
XM_011543675.1:c.16265G>T	XP_011541977.1:p.Gly5422Val
XM_011543676.1:c.16187G>T	XP_011541978.1:p.Gly5396Val
XM_011543677.1:c.13571G>T	XP_011541979.1:p.Gly4524Val
NM_032119.4:c.16268G>T MANE Select	NP_115495.3:p.Gly5423Val
XM_017009963.2:c.16289G>T	XP_016865452.1:p.Gly5430Val
XM_017009964.2:c.16286G>T	XP_016865453.1:p.Gly5429Val
XM_017009965.1:c.16286G>T	XP_016865454.1:p.Gly5429Val
XM_017009966.2:c.16208G>T	XP_016865455.1:p.Gly5403Val
XM_017009967.1:c.16193G>T	XP_016865456.1:p.Gly5398Val
XM_017009968.2:c.16109G>T	XP_016865457.1:p.Gly5370Val
XM_017009969.2:c.16289G>T	XP_016865458.1:p.Gly5430Val
XM_017009972.1:c.9407G>T	XP_016865461.1:p.Gly3136Val
XM_017009973.1:c.9386G>T	XP_016865462.1:p.Gly3129Val
NR_003149.2:n.16284G>T