Canonical Allele Identifier: CA360425540

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119291G>A (hg19) ; chr5:g.90823474G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823474G>A , CM000667.2:g.90823474G>A	GRCh38
NC_000005.9:g.90119291G>A , CM000667.1:g.90119291G>A	GRCh37
NC_000005.8:g.90155047G>A	NCBI36
NG_007083.1:g.269675G>A
NG_007083.2:g.299131G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16246G>A MANE Select	ENSP00000384582.2:p.Val5416Ile
ENST00000425867.3:c.5200G>A	ENSP00000392618.3:p.Val1734Ile
ENST00000638510.1:n.3513G>A
ENST00000639431.1:c.265+147265G>A	ENSP00000491057.1:n.265+147265G>A
ENST00000640061.1:n.128+1292G>A
ENST00000640407.1:c.2656G>A	ENSP00000491425.1:p.Val886Ile
ENST00000405460.6:c.16246G>A	ENSP00000384582.2:p.Val5416Ile
ENST00000425867.2:c.3229G>A	ENSP00000392618.2:p.Val1077Ile
NM_032119.3:c.16246G>A	NP_115495.3:p.Val5416Ile
NR_003149.1:n.16259G>A
XM_011543675.1:c.16243G>A	XP_011541977.1:p.Val5415Ile
XM_011543676.1:c.16165G>A	XP_011541978.1:p.Val5389Ile
XM_011543677.1:c.13549G>A	XP_011541979.1:p.Val4517Ile
NM_032119.4:c.16246G>A MANE Select	NP_115495.3:p.Val5416Ile
XM_017009963.2:c.16267G>A	XP_016865452.1:p.Val5423Ile
XM_017009964.2:c.16264G>A	XP_016865453.1:p.Val5422Ile
XM_017009965.1:c.16264G>A	XP_016865454.1:p.Val5422Ile
XM_017009966.2:c.16186G>A	XP_016865455.1:p.Val5396Ile
XM_017009967.1:c.16171G>A	XP_016865456.1:p.Val5391Ile
XM_017009968.2:c.16087G>A	XP_016865457.1:p.Val5363Ile
XM_017009969.2:c.16267G>A	XP_016865458.1:p.Val5423Ile
XM_017009972.1:c.9385G>A	XP_016865461.1:p.Val3129Ile
XM_017009973.1:c.9364G>A	XP_016865462.1:p.Val3122Ile
NR_003149.2:n.16262G>A