Canonical Allele Identifier: CA3341595

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90788139C>T , CM000667.2:g.90788139C>T	GRCh38
NC_000005.9:g.90083956C>T , CM000667.1:g.90083956C>T	GRCh37
NC_000005.8:g.90119712C>T	NCBI36
NG_007083.1:g.234340C>T
NG_007083.2:g.263796C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13722C>T MANE Select	NP_115495.3:p.Asp4574=
ENST00000405460.9:c.13722C>T MANE Select	ENSP00000384582.2:p.Asp4574=
NM_032119.3:c.13722C>T	NP_115495.3:p.Asp4574=
NR_003149.1:n.13735C>T
NR_003149.2:n.13738C>T
ENST00000405460.6:c.13722C>T	ENSP00000384582.2:p.Asp4574=
ENST00000425867.2:c.705C>T	ENSP00000392618.2:p.Asp235=
ENST00000425867.3:c.2676C>T	ENSP00000392618.3:p.Asp892=
ENST00000638510.1:n.989C>T
ENST00000638975.1:c.351C>T	ENSP00000492630.1:p.Asp117=
ENST00000639431.1:c.265+111930C>T	ENSP00000491057.1:n.265+111930C>T
ENST00000640407.1:c.132C>T	ENSP00000491425.1:p.Asp44=
XM_011543675.1:c.13719C>T	XP_011541977.1:p.Asp4573=
XM_011543676.1:c.13641C>T	XP_011541978.1:p.Asp4547=
XM_011543677.1:c.11025C>T	XP_011541979.1:p.Asp3675=
XM_011543678.1:c.13722C>T	XP_011541980.1:p.Asp4574=
XM_017009963.2:c.13743C>T	XP_016865452.1:p.Asp4581=
XM_017009964.2:c.13740C>T	XP_016865453.1:p.Asp4580=
XM_017009965.1:c.13740C>T	XP_016865454.1:p.Asp4580=
XM_017009966.2:c.13662C>T	XP_016865455.1:p.Asp4554=
XM_017009967.1:c.13647C>T	XP_016865456.1:p.Asp4549=
XM_017009968.2:c.13743C>T	XP_016865457.1:p.Asp4581=
XM_017009969.2:c.13743C>T	XP_016865458.1:p.Asp4581=
XM_017009970.2:c.13743C>T	XP_016865459.1:p.Asp4581=
XM_017009971.2:c.13743C>T	XP_016865460.1:p.Asp4581=
XM_017009972.1:c.6861C>T	XP_016865461.1:p.Asp2287=
XM_017009973.1:c.6840C>T	XP_016865462.1:p.Asp2280=