Canonical Allele Identifier: CA1562889865

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763308_90763309delinsAT , CM000667.2:g.90763308_90763309delinsAT	GRCh38
NC_000005.9:g.90059125_90059126delinsAT , CM000667.1:g.90059125_90059126delinsAT	GRCh37
NC_000005.8:g.90094881_90094882delinsAT	NCBI36
NG_007083.1:g.209509_209510delinsAT
NG_007083.2:g.238965_238966delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12124_12125delinsAT MANE Select	ENSP00000384582.2:p.Met4042=
ENST00000425867.3:c.1078_1079delinsAT	ENSP00000392618.3:p.Met360=
ENST00000639431.1:c.265+87099_265+87100delinsAT	ENSP00000491057.1:n.265+87099_265+87100delinsAT
ENST00000640464.1:n.2543_2544delinsAT
ENST00000640729.1:n.701_702delinsAT
ENST00000405460.6:c.12124_12125delinsAT	ENSP00000384582.2:p.Met4042=
NM_032119.3:c.12124_12125delinsAT	NP_115495.3:p.Met4042=
NR_003149.1:n.12137_12138delinsAT
XM_011543675.1:c.12121_12122delinsAT	XP_011541977.1:p.Met4041=
XM_011543676.1:c.12043_12044delinsAT	XP_011541978.1:p.Met4015=
XM_011543677.1:c.9427_9428delinsAT	XP_011541979.1:p.Met3143=
XM_011543678.1:c.12124_12125delinsAT	XP_011541980.1:p.Met4042=
NM_032119.4:c.12124_12125delinsAT MANE Select	NP_115495.3:p.Met4042=
XM_017009963.2:c.12145_12146delinsAT	XP_016865452.1:p.Met4049=
XM_017009964.2:c.12142_12143delinsAT	XP_016865453.1:p.Met4048=
XM_017009965.1:c.12142_12143delinsAT	XP_016865454.1:p.Met4048=
XM_017009966.2:c.12064_12065delinsAT	XP_016865455.1:p.Met4022=
XM_017009967.1:c.12049_12050delinsAT	XP_016865456.1:p.Met4017=
XM_017009968.2:c.12145_12146delinsAT	XP_016865457.1:p.Met4049=
XM_017009969.2:c.12145_12146delinsAT	XP_016865458.1:p.Met4049=
XM_017009970.2:c.12145_12146delinsAT	XP_016865459.1:p.Met4049=
XM_017009971.2:c.12145_12146delinsAT	XP_016865460.1:p.Met4049=
XM_017009972.1:c.5263_5264delinsAT	XP_016865461.1:p.Met1755=
XM_017009973.1:c.5242_5243delinsAT	XP_016865462.1:p.Met1748=
NR_003149.2:n.12140_12141delinsAT