Canonical Allele Identifier: CA360425587

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119316T>G (hg19) ; chr5:g.90823499T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823499T>G , CM000667.2:g.90823499T>G	GRCh38
NC_000005.9:g.90119316T>G , CM000667.1:g.90119316T>G	GRCh37
NC_000005.8:g.90155072T>G	NCBI36
NG_007083.1:g.269700T>G
NG_007083.2:g.299156T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16271T>G MANE Select	ENSP00000384582.2:p.Val5424Gly
ENST00000425867.3:c.5225T>G	ENSP00000392618.3:p.Val1742Gly
ENST00000638510.1:n.3538T>G
ENST00000639431.1:c.265+147290T>G	ENSP00000491057.1:n.265+147290T>G
ENST00000640061.1:n.128+1317T>G
ENST00000640407.1:c.2681T>G	ENSP00000491425.1:p.Val894Gly
ENST00000405460.6:c.16271T>G	ENSP00000384582.2:p.Val5424Gly
ENST00000425867.2:c.3254T>G	ENSP00000392618.2:p.Val1085Gly
NM_032119.3:c.16271T>G	NP_115495.3:p.Val5424Gly
NR_003149.1:n.16284T>G
XM_011543675.1:c.16268T>G	XP_011541977.1:p.Val5423Gly
XM_011543676.1:c.16190T>G	XP_011541978.1:p.Val5397Gly
XM_011543677.1:c.13574T>G	XP_011541979.1:p.Val4525Gly
NM_032119.4:c.16271T>G MANE Select	NP_115495.3:p.Val5424Gly
XM_017009963.2:c.16292T>G	XP_016865452.1:p.Val5431Gly
XM_017009964.2:c.16289T>G	XP_016865453.1:p.Val5430Gly
XM_017009965.1:c.16289T>G	XP_016865454.1:p.Val5430Gly
XM_017009966.2:c.16211T>G	XP_016865455.1:p.Val5404Gly
XM_017009967.1:c.16196T>G	XP_016865456.1:p.Val5399Gly
XM_017009968.2:c.16112T>G	XP_016865457.1:p.Val5371Gly
XM_017009969.2:c.16292T>G	XP_016865458.1:p.Val5431Gly
XM_017009972.1:c.9410T>G	XP_016865461.1:p.Val3137Gly
XM_017009973.1:c.9389T>G	XP_016865462.1:p.Val3130Gly
NR_003149.2:n.16287T>G