Canonical Allele Identifier: CA1562882086

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745659C= , CM000667.2:g.90745659C=	GRCh38
NC_000005.9:g.90041476C= , CM000667.1:g.90041476C=	GRCh37
NC_000005.8:g.90077232C=	NCBI36
NG_007083.1:g.191860C=
NG_007083.2:g.221316C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10838C= MANE Select	ENSP00000384582.2:p.Thr3613=
ENST00000639431.1:c.265+69450C=	ENSP00000491057.1:n.265+69450C=
ENST00000640374.1:n.3982C=
ENST00000640464.1:n.1257C=
ENST00000405460.6:c.10838C=	ENSP00000384582.2:p.Thr3613=
ENST00000509621.1:c.3535C=
NM_032119.3:c.10838C=	NP_115495.3:p.Thr3613=
NR_003149.1:n.10851C=
XM_011543675.1:c.10835C=	XP_011541977.1:p.Thr3612=
XM_011543676.1:c.10757C=	XP_011541978.1:p.Thr3586=
XM_011543677.1:c.8141C=	XP_011541979.1:p.Thr2714=
XM_011543678.1:c.10838C=	XP_011541980.1:p.Thr3613=
XM_011543679.1:c.*60C=	XP_011541981.1:n.*60C=
NM_032119.4:c.10838C= MANE Select	NP_115495.3:p.Thr3613=
XM_017009963.2:c.10859C=	XP_016865452.1:p.Thr3620=
XM_017009964.2:c.10856C=	XP_016865453.1:p.Thr3619=
XM_017009965.1:c.10856C=	XP_016865454.1:p.Thr3619=
XM_017009966.2:c.10778C=	XP_016865455.1:p.Thr3593=
XM_017009967.1:c.10763C=	XP_016865456.1:p.Thr3588=
XM_017009968.2:c.10859C=	XP_016865457.1:p.Thr3620=
XM_017009969.2:c.10859C=	XP_016865458.1:p.Thr3620=
XM_017009970.2:c.10859C=	XP_016865459.1:p.Thr3620=
XM_017009971.2:c.10859C=	XP_016865460.1:p.Thr3620=
XM_017009972.1:c.3977C=	XP_016865461.1:p.Thr1326=
XM_017009973.1:c.3956C=	XP_016865462.1:p.Thr1319=
XM_017009974.2:c.*60C=	XP_016865463.1:n.*60C=
NR_003149.2:n.10854C=