Canonical Allele Identifier: CA1562931276

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90853314T= , CM000667.2:g.90853314T=	GRCh38
NC_000005.9:g.90149131T= , CM000667.1:g.90149131T=	GRCh37
NC_000005.8:g.90184887T=	NCBI36
NG_007083.1:g.299515T=
NG_007083.2:g.328971T=

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17235T= MANE Select	NP_115495.3:p.Tyr5745=
ENST00000405460.9:c.17235T= MANE Select	ENSP00000384582.2:p.Tyr5745=
NM_032119.3:c.17235T=	NP_115495.3:p.Tyr5745=
NR_003149.1:n.17248T=
NR_003149.2:n.17251T=
ENST00000405460.6:c.17235T=	ENSP00000384582.2:p.Tyr5745=
ENST00000425867.2:c.4218T=	ENSP00000392618.2:p.Tyr1406=
ENST00000425867.3:c.6189T=	ENSP00000392618.3:p.Tyr2063=
ENST00000505845.2:n.426T=
ENST00000638510.1:n.4502T=
ENST00000638990.1:c.447T=
ENST00000639431.1:c.266-132030T=	ENSP00000491057.1:n.266-132030T=
ENST00000640407.1:c.3684T=	ENSP00000491425.1:n.3684T=
XM_011543675.1:c.17232T=	XP_011541977.1:p.Tyr5744=
XM_011543676.1:c.17154T=	XP_011541978.1:p.Tyr5718=
XM_011543677.1:c.14538T=	XP_011541979.1:p.Tyr4846=
XM_017009963.2:c.17256T=	XP_016865452.1:p.Tyr5752=
XM_017009964.2:c.17253T=	XP_016865453.1:p.Tyr5751=
XM_017009965.1:c.17253T=	XP_016865454.1:p.Tyr5751=
XM_017009966.2:c.17175T=	XP_016865455.1:p.Tyr5725=
XM_017009967.1:c.17160T=	XP_016865456.1:p.Tyr5720=
XM_017009968.2:c.17076T=	XP_016865457.1:p.Tyr5692=
XM_017009969.2:c.17256T=	XP_016865458.1:p.Tyr5752=
XM_017009972.1:c.10374T=	XP_016865461.1:p.Tyr3458=
XM_017009973.1:c.10353T=	XP_016865462.1:p.Tyr3451=