Canonical Allele Identifier: CA1562889878

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763347T= , CM000667.2:g.90763347T=	GRCh38
NC_000005.9:g.90059164T= , CM000667.1:g.90059164T=	GRCh37
NC_000005.8:g.90094920T=	NCBI36
NG_007083.1:g.209548T=
NG_007083.2:g.239004T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12163T= MANE Select	ENSP00000384582.2:p.Tyr4055=
ENST00000425867.3:c.1117T=	ENSP00000392618.3:p.Tyr373=
ENST00000639431.1:c.265+87138T=	ENSP00000491057.1:n.265+87138T=
ENST00000640464.1:n.2582T=
ENST00000640729.1:n.740T=
ENST00000405460.6:c.12163T=	ENSP00000384582.2:p.Tyr4055=
NM_032119.3:c.12163T=	NP_115495.3:p.Tyr4055=
NR_003149.1:n.12176T=
XM_011543675.1:c.12160T=	XP_011541977.1:p.Tyr4054=
XM_011543676.1:c.12082T=	XP_011541978.1:p.Tyr4028=
XM_011543677.1:c.9466T=	XP_011541979.1:p.Tyr3156=
XM_011543678.1:c.12163T=	XP_011541980.1:p.Tyr4055=
NM_032119.4:c.12163T= MANE Select	NP_115495.3:p.Tyr4055=
XM_017009963.2:c.12184T=	XP_016865452.1:p.Tyr4062=
XM_017009964.2:c.12181T=	XP_016865453.1:p.Tyr4061=
XM_017009965.1:c.12181T=	XP_016865454.1:p.Tyr4061=
XM_017009966.2:c.12103T=	XP_016865455.1:p.Tyr4035=
XM_017009967.1:c.12088T=	XP_016865456.1:p.Tyr4030=
XM_017009968.2:c.12184T=	XP_016865457.1:p.Tyr4062=
XM_017009969.2:c.12184T=	XP_016865458.1:p.Tyr4062=
XM_017009970.2:c.12184T=	XP_016865459.1:p.Tyr4062=
XM_017009971.2:c.12184T=	XP_016865460.1:p.Tyr4062=
XM_017009972.1:c.5302T=	XP_016865461.1:p.Tyr1768=
XM_017009973.1:c.5281T=	XP_016865462.1:p.Tyr1761=
NR_003149.2:n.12179T=