Canonical Allele Identifier: CA360377875

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059198G>C (hg19) ; chr5:g.90763381G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763381G>C , CM000667.2:g.90763381G>C	GRCh38
NC_000005.9:g.90059198G>C , CM000667.1:g.90059198G>C	GRCh37
NC_000005.8:g.90094954G>C	NCBI36
NG_007083.1:g.209582G>C
NG_007083.2:g.239038G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12197G>C MANE Select	ENSP00000384582.2:p.Gly4066Ala
ENST00000425867.3:c.1151G>C	ENSP00000392618.3:p.Gly384Ala
ENST00000639431.1:c.265+87172G>C	ENSP00000491057.1:n.265+87172G>C
ENST00000640464.1:n.2616G>C
ENST00000640729.1:n.774G>C
ENST00000405460.6:c.12197G>C	ENSP00000384582.2:p.Gly4066Ala
NM_032119.3:c.12197G>C	NP_115495.3:p.Gly4066Ala
NR_003149.1:n.12210G>C
XM_011543675.1:c.12194G>C	XP_011541977.1:p.Gly4065Ala
XM_011543676.1:c.12116G>C	XP_011541978.1:p.Gly4039Ala
XM_011543677.1:c.9500G>C	XP_011541979.1:p.Gly3167Ala
XM_011543678.1:c.12197G>C	XP_011541980.1:p.Gly4066Ala
NM_032119.4:c.12197G>C MANE Select	NP_115495.3:p.Gly4066Ala
XM_017009963.2:c.12218G>C	XP_016865452.1:p.Gly4073Ala
XM_017009964.2:c.12215G>C	XP_016865453.1:p.Gly4072Ala
XM_017009965.1:c.12215G>C	XP_016865454.1:p.Gly4072Ala
XM_017009966.2:c.12137G>C	XP_016865455.1:p.Gly4046Ala
XM_017009967.1:c.12122G>C	XP_016865456.1:p.Gly4041Ala
XM_017009968.2:c.12218G>C	XP_016865457.1:p.Gly4073Ala
XM_017009969.2:c.12218G>C	XP_016865458.1:p.Gly4073Ala
XM_017009970.2:c.12218G>C	XP_016865459.1:p.Gly4073Ala
XM_017009971.2:c.12218G>C	XP_016865460.1:p.Gly4073Ala
XM_017009972.1:c.5336G>C	XP_016865461.1:p.Gly1779Ala
XM_017009973.1:c.5315G>C	XP_016865462.1:p.Gly1772Ala
NR_003149.2:n.12213G>C