Canonical Allele Identifier: CA1562918263

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823480G= , CM000667.2:g.90823480G=	GRCh38
NC_000005.9:g.90119297G= , CM000667.1:g.90119297G=	GRCh37
NC_000005.8:g.90155053G=	NCBI36
NG_007083.1:g.269681G=
NG_007083.2:g.299137G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16252G= MANE Select	ENSP00000384582.2:p.Val5418=
ENST00000425867.3:c.5206G=	ENSP00000392618.3:p.Val1736=
ENST00000638510.1:n.3519G=
ENST00000639431.1:c.265+147271G=	ENSP00000491057.1:n.265+147271G=
ENST00000640061.1:n.128+1298G=
ENST00000640407.1:c.2662G=	ENSP00000491425.1:p.Val888=
ENST00000405460.6:c.16252G=	ENSP00000384582.2:p.Val5418=
ENST00000425867.2:c.3235G=	ENSP00000392618.2:p.Val1079=
NM_032119.3:c.16252G=	NP_115495.3:p.Val5418=
NR_003149.1:n.16265G=
XM_011543675.1:c.16249G=	XP_011541977.1:p.Val5417=
XM_011543676.1:c.16171G=	XP_011541978.1:p.Val5391=
XM_011543677.1:c.13555G=	XP_011541979.1:p.Val4519=
NM_032119.4:c.16252G= MANE Select	NP_115495.3:p.Val5418=
XM_017009963.2:c.16273G=	XP_016865452.1:p.Val5425=
XM_017009964.2:c.16270G=	XP_016865453.1:p.Val5424=
XM_017009965.1:c.16270G=	XP_016865454.1:p.Val5424=
XM_017009966.2:c.16192G=	XP_016865455.1:p.Val5398=
XM_017009967.1:c.16177G=	XP_016865456.1:p.Val5393=
XM_017009968.2:c.16093G=	XP_016865457.1:p.Val5365=
XM_017009969.2:c.16273G=	XP_016865458.1:p.Val5425=
XM_017009972.1:c.9391G=	XP_016865461.1:p.Val3131=
XM_017009973.1:c.9370G=	XP_016865462.1:p.Val3124=
NR_003149.2:n.16268G=