Canonical Allele Identifier: CA360425442

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90823427-C-A
• MyVariant Identifiers: chr5:g.90119244C>A (hg19) ; chr5:g.90823427C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823427C>A , CM000667.2:g.90823427C>A	GRCh38
NC_000005.9:g.90119244C>A , CM000667.1:g.90119244C>A	GRCh37
NC_000005.8:g.90155000C>A	NCBI36
NG_007083.1:g.269628C>A
NG_007083.2:g.299084C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16199C>A MANE Select	ENSP00000384582.2:p.Ala5400Asp
ENST00000425867.3:c.5153C>A	ENSP00000392618.3:p.Ala1718Asp
ENST00000638510.1:n.3466C>A
ENST00000639431.1:c.265+147218C>A	ENSP00000491057.1:n.265+147218C>A
ENST00000640061.1:n.128+1245C>A
ENST00000640407.1:c.2609C>A	ENSP00000491425.1:p.Ala870Asp
ENST00000405460.6:c.16199C>A	ENSP00000384582.2:p.Ala5400Asp
ENST00000425867.2:c.3182C>A	ENSP00000392618.2:p.Ala1061Asp
NM_032119.3:c.16199C>A	NP_115495.3:p.Ala5400Asp
NR_003149.1:n.16212C>A
XM_011543675.1:c.16196C>A	XP_011541977.1:p.Ala5399Asp
XM_011543676.1:c.16118C>A	XP_011541978.1:p.Ala5373Asp
XM_011543677.1:c.13502C>A	XP_011541979.1:p.Ala4501Asp
NM_032119.4:c.16199C>A MANE Select	NP_115495.3:p.Ala5400Asp
XM_017009963.2:c.16220C>A	XP_016865452.1:p.Ala5407Asp
XM_017009964.2:c.16217C>A	XP_016865453.1:p.Ala5406Asp
XM_017009965.1:c.16217C>A	XP_016865454.1:p.Ala5406Asp
XM_017009966.2:c.16139C>A	XP_016865455.1:p.Ala5380Asp
XM_017009967.1:c.16124C>A	XP_016865456.1:p.Ala5375Asp
XM_017009968.2:c.16040C>A	XP_016865457.1:p.Ala5347Asp
XM_017009969.2:c.16220C>A	XP_016865458.1:p.Ala5407Asp
XM_017009972.1:c.9338C>A	XP_016865461.1:p.Ala3113Asp
XM_017009973.1:c.9317C>A	XP_016865462.1:p.Ala3106Asp
NR_003149.2:n.16215C>A