Canonical Allele Identifier: CA122800380

Gene: ADGRV1

Linked Data

• dbSNP Id: rs997690585
• MyVariant Identifiers: chr5:g.90059164_90059165insA (hg19) ; chr5:g.90763347_90763348insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763348dup , CM000667.2:g.90763348dup	GRCh38
NC_000005.9:g.90059165dup , CM000667.1:g.90059165dup	GRCh37
NC_000005.8:g.90094921dup	NCBI36
NG_007083.1:g.209549dup
NG_007083.2:g.239005dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12164dup MANE Select	ENSP00000384582.2:p.Tyr4055Ter
ENST00000425867.3:c.1118dup	ENSP00000392618.3:p.Tyr373Ter
ENST00000639431.1:c.265+87139dup	ENSP00000491057.1:n.265+87139dup
ENST00000640464.1:n.2583dup
ENST00000640729.1:n.741dup
ENST00000405460.6:c.12164dup	ENSP00000384582.2:p.Tyr4055Ter
NM_032119.3:c.12164dup	NP_115495.3:p.Tyr4055Ter
NR_003149.1:n.12177dup
XM_011543675.1:c.12161dup	XP_011541977.1:p.Tyr4054Ter
XM_011543676.1:c.12083dup	XP_011541978.1:p.Tyr4028Ter
XM_011543677.1:c.9467dup	XP_011541979.1:p.Tyr3156Ter
XM_011543678.1:c.12164dup	XP_011541980.1:p.Tyr4055Ter
NM_032119.4:c.12164dup MANE Select	NP_115495.3:p.Tyr4055Ter
XM_017009963.2:c.12185dup	XP_016865452.1:p.Tyr4062Ter
XM_017009964.2:c.12182dup	XP_016865453.1:p.Tyr4061Ter
XM_017009965.1:c.12182dup	XP_016865454.1:p.Tyr4061Ter
XM_017009966.2:c.12104dup	XP_016865455.1:p.Tyr4035Ter
XM_017009967.1:c.12089dup	XP_016865456.1:p.Tyr4030Ter
XM_017009968.2:c.12185dup	XP_016865457.1:p.Tyr4062Ter
XM_017009969.2:c.12185dup	XP_016865458.1:p.Tyr4062Ter
XM_017009970.2:c.12185dup	XP_016865459.1:p.Tyr4062Ter
XM_017009971.2:c.12185dup	XP_016865460.1:p.Tyr4062Ter
XM_017009972.1:c.5303dup	XP_016865461.1:p.Tyr1768Ter
XM_017009973.1:c.5282dup	XP_016865462.1:p.Tyr1761Ter
NR_003149.2:n.12180dup