Canonical Allele Identifier: CA1562895823

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90776518T= , CM000667.2:g.90776518T=	GRCh38
NC_000005.9:g.90072335T= , CM000667.1:g.90072335T=	GRCh37
NC_000005.8:g.90108091T=	NCBI36
NG_007083.1:g.222719T=
NG_007083.2:g.252175T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.12469T= MANE Select	ENSP00000384582.2:p.Ser4157=
ENST00000425867.3:c.1423T=	ENSP00000392618.3:p.Ser475=
ENST00000639431.1:c.265+100309T=	ENSP00000491057.1:n.265+100309T=
ENST00000640464.1:n.2888T=
ENST00000640729.1:n.1046T=
ENST00000405460.6:c.12469T=	ENSP00000384582.2:p.Ser4157=
NM_032119.3:c.12469T=	NP_115495.3:p.Ser4157=
NR_003149.1:n.12482T=
XM_011543675.1:c.12466T=	XP_011541977.1:p.Ser4156=
XM_011543676.1:c.12388T=	XP_011541978.1:p.Ser4130=
XM_011543677.1:c.9772T=	XP_011541979.1:p.Ser3258=
XM_011543678.1:c.12469T=	XP_011541980.1:p.Ser4157=
NM_032119.4:c.12469T= MANE Select	NP_115495.3:p.Ser4157=
XM_017009963.2:c.12490T=	XP_016865452.1:p.Ser4164=
XM_017009964.2:c.12487T=	XP_016865453.1:p.Ser4163=
XM_017009965.1:c.12487T=	XP_016865454.1:p.Ser4163=
XM_017009966.2:c.12409T=	XP_016865455.1:p.Ser4137=
XM_017009967.1:c.12394T=	XP_016865456.1:p.Ser4132=
XM_017009968.2:c.12490T=	XP_016865457.1:p.Ser4164=
XM_017009969.2:c.12490T=	XP_016865458.1:p.Ser4164=
XM_017009970.2:c.12490T=	XP_016865459.1:p.Ser4164=
XM_017009971.2:c.12490T=	XP_016865460.1:p.Ser4164=
XM_017009972.1:c.5608T=	XP_016865461.1:p.Ser1870=
XM_017009973.1:c.5587T=	XP_016865462.1:p.Ser1863=
NR_003149.2:n.12485T=