Canonical Allele Identifier: CA360425534

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90823471-A-G
• MyVariant Identifiers: chr5:g.90119288A>G (hg19) ; chr5:g.90823471A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823471A>G , CM000667.2:g.90823471A>G	GRCh38
NC_000005.9:g.90119288A>G , CM000667.1:g.90119288A>G	GRCh37
NC_000005.8:g.90155044A>G	NCBI36
NG_007083.1:g.269672A>G
NG_007083.2:g.299128A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16243A>G MANE Select	ENSP00000384582.2:p.Thr5415Ala
ENST00000425867.3:c.5197A>G	ENSP00000392618.3:p.Thr1733Ala
ENST00000638510.1:n.3510A>G
ENST00000639431.1:c.265+147262A>G	ENSP00000491057.1:n.265+147262A>G
ENST00000640061.1:n.128+1289A>G
ENST00000640407.1:c.2653A>G	ENSP00000491425.1:p.Thr885Ala
ENST00000405460.6:c.16243A>G	ENSP00000384582.2:p.Thr5415Ala
ENST00000425867.2:c.3226A>G	ENSP00000392618.2:p.Thr1076Ala
NM_032119.3:c.16243A>G	NP_115495.3:p.Thr5415Ala
NR_003149.1:n.16256A>G
XM_011543675.1:c.16240A>G	XP_011541977.1:p.Thr5414Ala
XM_011543676.1:c.16162A>G	XP_011541978.1:p.Thr5388Ala
XM_011543677.1:c.13546A>G	XP_011541979.1:p.Thr4516Ala
NM_032119.4:c.16243A>G MANE Select	NP_115495.3:p.Thr5415Ala
XM_017009963.2:c.16264A>G	XP_016865452.1:p.Thr5422Ala
XM_017009964.2:c.16261A>G	XP_016865453.1:p.Thr5421Ala
XM_017009965.1:c.16261A>G	XP_016865454.1:p.Thr5421Ala
XM_017009966.2:c.16183A>G	XP_016865455.1:p.Thr5395Ala
XM_017009967.1:c.16168A>G	XP_016865456.1:p.Thr5390Ala
XM_017009968.2:c.16084A>G	XP_016865457.1:p.Thr5362Ala
XM_017009969.2:c.16264A>G	XP_016865458.1:p.Thr5422Ala
XM_017009972.1:c.9382A>G	XP_016865461.1:p.Thr3128Ala
XM_017009973.1:c.9361A>G	XP_016865462.1:p.Thr3121Ala
NR_003149.2:n.16259A>G