Canonical Allele Identifier: CA445467599

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90791196-G-T
• MyVariant Identifiers: chr5:g.90087013G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791196G>T , CM000667.2:g.90791196G>T	GRCh38
NC_000005.9:g.90087013G>T , CM000667.1:g.90087013G>T	GRCh37
NC_000005.8:g.90122769G>T	NCBI36
NG_007083.1:g.237397G>T
NG_007083.2:g.266853G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14367G>T MANE Select	ENSP00000384582.2:p.Arg4789=
ENST00000425867.3:c.3321G>T	ENSP00000392618.3:p.Arg1107=
ENST00000507314.2:c.42G>T	ENSP00000491299.1:p.Arg14=
ENST00000638510.1:n.1634G>T
ENST00000638585.1:n.133G>T
ENST00000638975.1:c.996G>T	ENSP00000492630.1:p.Arg332=
ENST00000639431.1:c.265+114987G>T	ENSP00000491057.1:n.265+114987G>T
ENST00000640407.1:c.777G>T	ENSP00000491425.1:p.Arg259=
ENST00000405460.6:c.14367G>T	ENSP00000384582.2:p.Arg4789=
ENST00000425867.2:c.1350G>T	ENSP00000392618.2:p.Arg450=
ENST00000507314.1:n.42G>T
NM_032119.3:c.14367G>T	NP_115495.3:p.Arg4789=
NR_003149.1:n.14380G>T
XM_011543675.1:c.14364G>T	XP_011541977.1:p.Arg4788=
XM_011543676.1:c.14286G>T	XP_011541978.1:p.Arg4762=
XM_011543677.1:c.11670G>T	XP_011541979.1:p.Arg3890=
XM_011543678.1:c.14367G>T	XP_011541980.1:p.Arg4789=
NM_032119.4:c.14367G>T MANE Select	NP_115495.3:p.Arg4789=
XM_017009963.2:c.14388G>T	XP_016865452.1:p.Arg4796=
XM_017009964.2:c.14385G>T	XP_016865453.1:p.Arg4795=
XM_017009965.1:c.14385G>T	XP_016865454.1:p.Arg4795=
XM_017009966.2:c.14307G>T	XP_016865455.1:p.Arg4769=
XM_017009967.1:c.14292G>T	XP_016865456.1:p.Arg4764=
XM_017009968.2:c.14388G>T	XP_016865457.1:p.Arg4796=
XM_017009969.2:c.14388G>T	XP_016865458.1:p.Arg4796=
XM_017009970.2:c.14388G>T	XP_016865459.1:p.Arg4796=
XM_017009971.2:c.14388G>T	XP_016865460.1:p.Arg4796=
XM_017009972.1:c.7506G>T	XP_016865461.1:p.Arg2502=
XM_017009973.1:c.7485G>T	XP_016865462.1:p.Arg2495=
NR_003149.2:n.14383G>T