Canonical Allele Identifier: CA360425542

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119292T>G (hg19) ; chr5:g.90823475T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823475T>G , CM000667.2:g.90823475T>G	GRCh38
NC_000005.9:g.90119292T>G , CM000667.1:g.90119292T>G	GRCh37
NC_000005.8:g.90155048T>G	NCBI36
NG_007083.1:g.269676T>G
NG_007083.2:g.299132T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16247T>G MANE Select	ENSP00000384582.2:p.Val5416Gly
ENST00000425867.3:c.5201T>G	ENSP00000392618.3:p.Val1734Gly
ENST00000638510.1:n.3514T>G
ENST00000639431.1:c.265+147266T>G	ENSP00000491057.1:n.265+147266T>G
ENST00000640061.1:n.128+1293T>G
ENST00000640407.1:c.2657T>G	ENSP00000491425.1:p.Val886Gly
ENST00000405460.6:c.16247T>G	ENSP00000384582.2:p.Val5416Gly
ENST00000425867.2:c.3230T>G	ENSP00000392618.2:p.Val1077Gly
NM_032119.3:c.16247T>G	NP_115495.3:p.Val5416Gly
NR_003149.1:n.16260T>G
XM_011543675.1:c.16244T>G	XP_011541977.1:p.Val5415Gly
XM_011543676.1:c.16166T>G	XP_011541978.1:p.Val5389Gly
XM_011543677.1:c.13550T>G	XP_011541979.1:p.Val4517Gly
NM_032119.4:c.16247T>G MANE Select	NP_115495.3:p.Val5416Gly
XM_017009963.2:c.16268T>G	XP_016865452.1:p.Val5423Gly
XM_017009964.2:c.16265T>G	XP_016865453.1:p.Val5422Gly
XM_017009965.1:c.16265T>G	XP_016865454.1:p.Val5422Gly
XM_017009966.2:c.16187T>G	XP_016865455.1:p.Val5396Gly
XM_017009967.1:c.16172T>G	XP_016865456.1:p.Val5391Gly
XM_017009968.2:c.16088T>G	XP_016865457.1:p.Val5363Gly
XM_017009969.2:c.16268T>G	XP_016865458.1:p.Val5423Gly
XM_017009972.1:c.9386T>G	XP_016865461.1:p.Val3129Gly
XM_017009973.1:c.9365T>G	XP_016865462.1:p.Val3122Gly
NR_003149.2:n.16263T>G