Canonical Allele Identifier: CA1562873565

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725621A= , CM000667.2:g.90725621A=	GRCh38
NC_000005.9:g.90021438A= , CM000667.1:g.90021438A=	GRCh37
NC_000005.8:g.90057194A=	NCBI36
NG_007083.1:g.171822A=
NG_007083.2:g.201278A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10126A= MANE Select	ENSP00000384582.2:p.Ile3376=
ENST00000639431.1:c.265+49412A=	ENSP00000491057.1:n.265+49412A=
ENST00000640374.1:n.3270A=
ENST00000640464.1:n.545A=
ENST00000405460.6:c.10126A=	ENSP00000384582.2:p.Ile3376=
ENST00000509621.1:c.2823A=
NM_032119.3:c.10126A=	NP_115495.3:p.Ile3376=
NR_003149.1:n.10139A=
XM_011543675.1:c.10123A=	XP_011541977.1:p.Ile3375=
XM_011543676.1:c.10045A=	XP_011541978.1:p.Ile3349=
XM_011543677.1:c.7429A=	XP_011541979.1:p.Ile2477=
XM_011543678.1:c.10126A=	XP_011541980.1:p.Ile3376=
XM_011543679.1:c.10126A=	XP_011541981.1:p.Ile3376=
XR_948560.1:n.272-9812T=
NM_032119.4:c.10126A= MANE Select	NP_115495.3:p.Ile3376=
XM_017009963.2:c.10147A=	XP_016865452.1:p.Ile3383=
XM_017009964.2:c.10144A=	XP_016865453.1:p.Ile3382=
XM_017009965.1:c.10144A=	XP_016865454.1:p.Ile3382=
XM_017009966.2:c.10066A=	XP_016865455.1:p.Ile3356=
XM_017009967.1:c.10051A=	XP_016865456.1:p.Ile3351=
XM_017009968.2:c.10147A=	XP_016865457.1:p.Ile3383=
XM_017009969.2:c.10147A=	XP_016865458.1:p.Ile3383=
XM_017009970.2:c.10147A=	XP_016865459.1:p.Ile3383=
XM_017009971.2:c.10147A=	XP_016865460.1:p.Ile3383=
XM_017009972.1:c.3265A=	XP_016865461.1:p.Ile1089=
XM_017009973.1:c.3244A=	XP_016865462.1:p.Ile1082=
XM_017009974.2:c.10147A=	XP_016865463.1:p.Ile3383=
XR_001742802.1:n.2523-9812T=
NR_003149.2:n.10142A=