Canonical Allele Identifier: CA360425589

Gene: ADGRV1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16271T>A MANE Select	ENSP00000384582.2:p.Val5424Glu
ENST00000425867.3:c.5225T>A	ENSP00000392618.3:p.Val1742Glu
ENST00000638510.1:n.3538T>A
ENST00000639431.1:c.265+147290T>A	ENSP00000491057.1:n.265+147290T>A
ENST00000640061.1:n.128+1317T>A
ENST00000640407.1:c.2681T>A	ENSP00000491425.1:p.Val894Glu
ENST00000405460.6:c.16271T>A	ENSP00000384582.2:p.Val5424Glu
ENST00000425867.2:c.3254T>A	ENSP00000392618.2:p.Val1085Glu
NM_032119.3:c.16271T>A	NP_115495.3:p.Val5424Glu
NR_003149.1:n.16284T>A
XM_011543675.1:c.16268T>A	XP_011541977.1:p.Val5423Glu
XM_011543676.1:c.16190T>A	XP_011541978.1:p.Val5397Glu
XM_011543677.1:c.13574T>A	XP_011541979.1:p.Val4525Glu
NM_032119.4:c.16271T>A MANE Select	NP_115495.3:p.Val5424Glu
XM_017009963.2:c.16292T>A	XP_016865452.1:p.Val5431Glu
XM_017009964.2:c.16289T>A	XP_016865453.1:p.Val5430Glu
XM_017009965.1:c.16289T>A	XP_016865454.1:p.Val5430Glu
XM_017009966.2:c.16211T>A	XP_016865455.1:p.Val5404Glu
XM_017009967.1:c.16196T>A	XP_016865456.1:p.Val5399Glu
XM_017009968.2:c.16112T>A	XP_016865457.1:p.Val5371Glu
XM_017009969.2:c.16292T>A	XP_016865458.1:p.Val5431Glu
XM_017009972.1:c.9410T>A	XP_016865461.1:p.Val3137Glu
XM_017009973.1:c.9389T>A	XP_016865462.1:p.Val3130Glu
NR_003149.2:n.16287T>A