Canonical Allele Identifier: CA1562888123

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90759569T= , CM000667.2:g.90759569T=	GRCh38
NC_000005.9:g.90055386T= , CM000667.1:g.90055386T=	GRCh37
NC_000005.8:g.90091142T=	NCBI36
NG_007083.1:g.205770T=
NG_007083.2:g.235226T=

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12101T= MANE Select	NP_115495.3:p.Phe4034=
ENST00000405460.9:c.12101T= MANE Select	ENSP00000384582.2:p.Phe4034=
NM_032119.3:c.12101T=	NP_115495.3:p.Phe4034=
NR_003149.1:n.12114T=
NR_003149.2:n.12117T=
ENST00000405460.6:c.12101T=	ENSP00000384582.2:p.Phe4034=
ENST00000425867.3:c.1055T=	ENSP00000392618.3:p.Phe352=
ENST00000509621.1:c.4798T=
ENST00000639431.1:c.265+83360T=	ENSP00000491057.1:n.265+83360T=
ENST00000639884.1:n.755T=
ENST00000640374.1:n.5068T=
ENST00000640464.1:n.2520T=
XM_011543675.1:c.12098T=	XP_011541977.1:p.Phe4033=
XM_011543676.1:c.12020T=	XP_011541978.1:p.Phe4007=
XM_011543677.1:c.9404T=	XP_011541979.1:p.Phe3135=
XM_011543678.1:c.12101T=	XP_011541980.1:p.Phe4034=
XM_017009963.2:c.12122T=	XP_016865452.1:p.Phe4041=
XM_017009964.2:c.12119T=	XP_016865453.1:p.Phe4040=
XM_017009965.1:c.12119T=	XP_016865454.1:p.Phe4040=
XM_017009966.2:c.12041T=	XP_016865455.1:p.Phe4014=
XM_017009967.1:c.12026T=	XP_016865456.1:p.Phe4009=
XM_017009968.2:c.12122T=	XP_016865457.1:p.Phe4041=
XM_017009969.2:c.12122T=	XP_016865458.1:p.Phe4041=
XM_017009970.2:c.12122T=	XP_016865459.1:p.Phe4041=
XM_017009971.2:c.12122T=	XP_016865460.1:p.Phe4041=
XM_017009972.1:c.5240T=	XP_016865461.1:p.Phe1747=
XM_017009973.1:c.5219T=	XP_016865462.1:p.Phe1740=