Canonical Allele Identifier: CA445468256

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106816A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810999A>C , CM000667.2:g.90810999A>C	GRCh38
NC_000005.9:g.90106816A>C , CM000667.1:g.90106816A>C	GRCh37
NC_000005.8:g.90142572A>C	NCBI36
NG_007083.1:g.257200A>C
NG_007083.2:g.286656A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15739A>C MANE Select	ENSP00000384582.2:p.Arg5247=
ENST00000425867.3:c.4693A>C	ENSP00000392618.3:p.Arg1565=
ENST00000638510.1:n.3006A>C
ENST00000639431.1:c.265+134790A>C	ENSP00000491057.1:n.265+134790A>C
ENST00000640407.1:c.2149A>C	ENSP00000491425.1:p.Arg717=
ENST00000405460.6:c.15739A>C	ENSP00000384582.2:p.Arg5247=
ENST00000425867.2:c.2722A>C	ENSP00000392618.2:p.Arg908=
NM_032119.3:c.15739A>C	NP_115495.3:p.Arg5247=
NR_003149.1:n.15752A>C
XM_011543675.1:c.15736A>C	XP_011541977.1:p.Arg5246=
XM_011543676.1:c.15658A>C	XP_011541978.1:p.Arg5220=
XM_011543677.1:c.13042A>C	XP_011541979.1:p.Arg4348=
NM_032119.4:c.15739A>C MANE Select	NP_115495.3:p.Arg5247=
XM_017009963.2:c.15760A>C	XP_016865452.1:p.Arg5254=
XM_017009964.2:c.15757A>C	XP_016865453.1:p.Arg5253=
XM_017009965.1:c.15757A>C	XP_016865454.1:p.Arg5253=
XM_017009966.2:c.15679A>C	XP_016865455.1:p.Arg5227=
XM_017009967.1:c.15664A>C	XP_016865456.1:p.Arg5222=
XM_017009968.2:c.15580A>C	XP_016865457.1:p.Arg5194=
XM_017009969.2:c.15760A>C	XP_016865458.1:p.Arg5254=
XM_017009972.1:c.8878A>C	XP_016865461.1:p.Arg2960=
XM_017009973.1:c.8857A>C	XP_016865462.1:p.Arg2953=
NR_003149.2:n.15755A>C