Canonical Allele Identifier: CA3341496

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90783185T>C , CM000667.2:g.90783185T>C	GRCh38
NC_000005.9:g.90079002T>C , CM000667.1:g.90079002T>C	GRCh37
NC_000005.8:g.90114758T>C	NCBI36
NG_007083.1:g.229386T>C
NG_007083.2:g.258842T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13293T>C MANE Select	NP_115495.3:p.Tyr4431=
ENST00000405460.9:c.13293T>C MANE Select	ENSP00000384582.2:p.Tyr4431=
NM_032119.3:c.13293T>C	NP_115495.3:p.Tyr4431=
NR_003149.1:n.13306T>C
NR_003149.2:n.13309T>C
ENST00000405460.6:c.13293T>C	ENSP00000384582.2:p.Tyr4431=
ENST00000425867.2:c.276T>C	ENSP00000392618.2:p.Tyr92=
ENST00000425867.3:c.2247T>C	ENSP00000392618.3:p.Tyr749=
ENST00000638510.1:n.560T>C
ENST00000639431.1:c.265+106976T>C	ENSP00000491057.1:n.265+106976T>C
XM_011543675.1:c.13290T>C	XP_011541977.1:p.Tyr4430=
XM_011543676.1:c.13212T>C	XP_011541978.1:p.Tyr4404=
XM_011543677.1:c.10596T>C	XP_011541979.1:p.Tyr3532=
XM_011543678.1:c.13293T>C	XP_011541980.1:p.Tyr4431=
XM_017009963.2:c.13314T>C	XP_016865452.1:p.Tyr4438=
XM_017009964.2:c.13311T>C	XP_016865453.1:p.Tyr4437=
XM_017009965.1:c.13311T>C	XP_016865454.1:p.Tyr4437=
XM_017009966.2:c.13233T>C	XP_016865455.1:p.Tyr4411=
XM_017009967.1:c.13218T>C	XP_016865456.1:p.Tyr4406=
XM_017009968.2:c.13314T>C	XP_016865457.1:p.Tyr4438=
XM_017009969.2:c.13314T>C	XP_016865458.1:p.Tyr4438=
XM_017009970.2:c.13314T>C	XP_016865459.1:p.Tyr4438=
XM_017009971.2:c.13314T>C	XP_016865460.1:p.Tyr4438=
XM_017009972.1:c.6432T>C	XP_016865461.1:p.Tyr2144=
XM_017009973.1:c.6411T>C	XP_016865462.1:p.Tyr2137=