Canonical Allele Identifier: CA360425553

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119300C>G (hg19) ; chr5:g.90823483C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823483C>G , CM000667.2:g.90823483C>G	GRCh38
NC_000005.9:g.90119300C>G , CM000667.1:g.90119300C>G	GRCh37
NC_000005.8:g.90155056C>G	NCBI36
NG_007083.1:g.269684C>G
NG_007083.2:g.299140C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16255C>G MANE Select	ENSP00000384582.2:p.Leu5419Val
ENST00000425867.3:c.5209C>G	ENSP00000392618.3:p.Leu1737Val
ENST00000638510.1:n.3522C>G
ENST00000639431.1:c.265+147274C>G	ENSP00000491057.1:n.265+147274C>G
ENST00000640061.1:n.128+1301C>G
ENST00000640407.1:c.2665C>G	ENSP00000491425.1:p.Leu889Val
ENST00000405460.6:c.16255C>G	ENSP00000384582.2:p.Leu5419Val
ENST00000425867.2:c.3238C>G	ENSP00000392618.2:p.Leu1080Val
NM_032119.3:c.16255C>G	NP_115495.3:p.Leu5419Val
NR_003149.1:n.16268C>G
XM_011543675.1:c.16252C>G	XP_011541977.1:p.Leu5418Val
XM_011543676.1:c.16174C>G	XP_011541978.1:p.Leu5392Val
XM_011543677.1:c.13558C>G	XP_011541979.1:p.Leu4520Val
NM_032119.4:c.16255C>G MANE Select	NP_115495.3:p.Leu5419Val
XM_017009963.2:c.16276C>G	XP_016865452.1:p.Leu5426Val
XM_017009964.2:c.16273C>G	XP_016865453.1:p.Leu5425Val
XM_017009965.1:c.16273C>G	XP_016865454.1:p.Leu5425Val
XM_017009966.2:c.16195C>G	XP_016865455.1:p.Leu5399Val
XM_017009967.1:c.16180C>G	XP_016865456.1:p.Leu5394Val
XM_017009968.2:c.16096C>G	XP_016865457.1:p.Leu5366Val
XM_017009969.2:c.16276C>G	XP_016865458.1:p.Leu5426Val
XM_017009972.1:c.9394C>G	XP_016865461.1:p.Leu3132Val
XM_017009973.1:c.9373C>G	XP_016865462.1:p.Leu3125Val
NR_003149.2:n.16271C>G