Canonical Allele Identifier: CA360425736

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119388T>G (hg19) ; chr5:g.90823571T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823571T>G , CM000667.2:g.90823571T>G	GRCh38
NC_000005.9:g.90119388T>G , CM000667.1:g.90119388T>G	GRCh37
NC_000005.8:g.90155144T>G	NCBI36
NG_007083.1:g.269772T>G
NG_007083.2:g.299228T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16343T>G MANE Select	ENSP00000384582.2:p.Ile5448Ser
ENST00000425867.3:c.5297T>G	ENSP00000392618.3:p.Ile1766Ser
ENST00000638510.1:n.3610T>G
ENST00000639431.1:c.265+147362T>G	ENSP00000491057.1:n.265+147362T>G
ENST00000640061.1:n.128+1389T>G
ENST00000640407.1:c.2753T>G	ENSP00000491425.1:p.Ile918Ser
ENST00000405460.6:c.16343T>G	ENSP00000384582.2:p.Ile5448Ser
ENST00000425867.2:c.3326T>G	ENSP00000392618.2:p.Ile1109Ser
NM_032119.3:c.16343T>G	NP_115495.3:p.Ile5448Ser
NR_003149.1:n.16356T>G
XM_011543675.1:c.16340T>G	XP_011541977.1:p.Ile5447Ser
XM_011543676.1:c.16262T>G	XP_011541978.1:p.Ile5421Ser
XM_011543677.1:c.13646T>G	XP_011541979.1:p.Ile4549Ser
NM_032119.4:c.16343T>G MANE Select	NP_115495.3:p.Ile5448Ser
XM_017009963.2:c.16364T>G	XP_016865452.1:p.Ile5455Ser
XM_017009964.2:c.16361T>G	XP_016865453.1:p.Ile5454Ser
XM_017009965.1:c.16361T>G	XP_016865454.1:p.Ile5454Ser
XM_017009966.2:c.16283T>G	XP_016865455.1:p.Ile5428Ser
XM_017009967.1:c.16268T>G	XP_016865456.1:p.Ile5423Ser
XM_017009968.2:c.16184T>G	XP_016865457.1:p.Ile5395Ser
XM_017009969.2:c.16364T>G	XP_016865458.1:p.Ile5455Ser
XM_017009972.1:c.9482T>G	XP_016865461.1:p.Ile3161Ser
XM_017009973.1:c.9461T>G	XP_016865462.1:p.Ile3154Ser
NR_003149.2:n.16359T>G