Canonical Allele Identifier: CA360410726

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106826G>C (hg19) ; chr5:g.90811009G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811009G>C , CM000667.2:g.90811009G>C	GRCh38
NC_000005.9:g.90106826G>C , CM000667.1:g.90106826G>C	GRCh37
NC_000005.8:g.90142582G>C	NCBI36
NG_007083.1:g.257210G>C
NG_007083.2:g.286666G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15749G>C MANE Select	ENSP00000384582.2:p.Gly5250Ala
ENST00000425867.3:c.4703G>C	ENSP00000392618.3:p.Gly1568Ala
ENST00000638510.1:n.3016G>C
ENST00000639431.1:c.265+134800G>C	ENSP00000491057.1:n.265+134800G>C
ENST00000640407.1:c.2159G>C	ENSP00000491425.1:p.Gly720Ala
ENST00000405460.6:c.15749G>C	ENSP00000384582.2:p.Gly5250Ala
ENST00000425867.2:c.2732G>C	ENSP00000392618.2:p.Gly911Ala
NM_032119.3:c.15749G>C	NP_115495.3:p.Gly5250Ala
NR_003149.1:n.15762G>C
XM_011543675.1:c.15746G>C	XP_011541977.1:p.Gly5249Ala
XM_011543676.1:c.15668G>C	XP_011541978.1:p.Gly5223Ala
XM_011543677.1:c.13052G>C	XP_011541979.1:p.Gly4351Ala
NM_032119.4:c.15749G>C MANE Select	NP_115495.3:p.Gly5250Ala
XM_017009963.2:c.15770G>C	XP_016865452.1:p.Gly5257Ala
XM_017009964.2:c.15767G>C	XP_016865453.1:p.Gly5256Ala
XM_017009965.1:c.15767G>C	XP_016865454.1:p.Gly5256Ala
XM_017009966.2:c.15689G>C	XP_016865455.1:p.Gly5230Ala
XM_017009967.1:c.15674G>C	XP_016865456.1:p.Gly5225Ala
XM_017009968.2:c.15590G>C	XP_016865457.1:p.Gly5197Ala
XM_017009969.2:c.15770G>C	XP_016865458.1:p.Gly5257Ala
XM_017009972.1:c.8888G>C	XP_016865461.1:p.Gly2963Ala
XM_017009973.1:c.8867G>C	XP_016865462.1:p.Gly2956Ala
NR_003149.2:n.15765G>C