Canonical Allele Identifier: CA445436557

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119302C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823485C>T , CM000667.2:g.90823485C>T	GRCh38
NC_000005.9:g.90119302C>T , CM000667.1:g.90119302C>T	GRCh37
NC_000005.8:g.90155058C>T	NCBI36
NG_007083.1:g.269686C>T
NG_007083.2:g.299142C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16257C>T MANE Select	ENSP00000384582.2:p.Leu5419=
ENST00000425867.3:c.5211C>T	ENSP00000392618.3:p.Leu1737=
ENST00000638510.1:n.3524C>T
ENST00000639431.1:c.265+147276C>T	ENSP00000491057.1:n.265+147276C>T
ENST00000640061.1:n.128+1303C>T
ENST00000640407.1:c.2667C>T	ENSP00000491425.1:p.Leu889=
ENST00000405460.6:c.16257C>T	ENSP00000384582.2:p.Leu5419=
ENST00000425867.2:c.3240C>T	ENSP00000392618.2:p.Leu1080=
NM_032119.3:c.16257C>T	NP_115495.3:p.Leu5419=
NR_003149.1:n.16270C>T
XM_011543675.1:c.16254C>T	XP_011541977.1:p.Leu5418=
XM_011543676.1:c.16176C>T	XP_011541978.1:p.Leu5392=
XM_011543677.1:c.13560C>T	XP_011541979.1:p.Leu4520=
NM_032119.4:c.16257C>T MANE Select	NP_115495.3:p.Leu5419=
XM_017009963.2:c.16278C>T	XP_016865452.1:p.Leu5426=
XM_017009964.2:c.16275C>T	XP_016865453.1:p.Leu5425=
XM_017009965.1:c.16275C>T	XP_016865454.1:p.Leu5425=
XM_017009966.2:c.16197C>T	XP_016865455.1:p.Leu5399=
XM_017009967.1:c.16182C>T	XP_016865456.1:p.Leu5394=
XM_017009968.2:c.16098C>T	XP_016865457.1:p.Leu5366=
XM_017009969.2:c.16278C>T	XP_016865458.1:p.Leu5426=
XM_017009972.1:c.9396C>T	XP_016865461.1:p.Leu3132=
XM_017009973.1:c.9375C>T	XP_016865462.1:p.Leu3125=
NR_003149.2:n.16273C>T