Canonical Allele Identifier: CA360425580

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119312G>C (hg19) ; chr5:g.90823495G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823495G>C , CM000667.2:g.90823495G>C	GRCh38
NC_000005.9:g.90119312G>C , CM000667.1:g.90119312G>C	GRCh37
NC_000005.8:g.90155068G>C	NCBI36
NG_007083.1:g.269696G>C
NG_007083.2:g.299152G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16267G>C MANE Select	ENSP00000384582.2:p.Gly5423Arg
ENST00000425867.3:c.5221G>C	ENSP00000392618.3:p.Gly1741Arg
ENST00000638510.1:n.3534G>C
ENST00000639431.1:c.265+147286G>C	ENSP00000491057.1:n.265+147286G>C
ENST00000640061.1:n.128+1313G>C
ENST00000640407.1:c.2677G>C	ENSP00000491425.1:p.Gly893Arg
ENST00000405460.6:c.16267G>C	ENSP00000384582.2:p.Gly5423Arg
ENST00000425867.2:c.3250G>C	ENSP00000392618.2:p.Gly1084Arg
NM_032119.3:c.16267G>C	NP_115495.3:p.Gly5423Arg
NR_003149.1:n.16280G>C
XM_011543675.1:c.16264G>C	XP_011541977.1:p.Gly5422Arg
XM_011543676.1:c.16186G>C	XP_011541978.1:p.Gly5396Arg
XM_011543677.1:c.13570G>C	XP_011541979.1:p.Gly4524Arg
NM_032119.4:c.16267G>C MANE Select	NP_115495.3:p.Gly5423Arg
XM_017009963.2:c.16288G>C	XP_016865452.1:p.Gly5430Arg
XM_017009964.2:c.16285G>C	XP_016865453.1:p.Gly5429Arg
XM_017009965.1:c.16285G>C	XP_016865454.1:p.Gly5429Arg
XM_017009966.2:c.16207G>C	XP_016865455.1:p.Gly5403Arg
XM_017009967.1:c.16192G>C	XP_016865456.1:p.Gly5398Arg
XM_017009968.2:c.16108G>C	XP_016865457.1:p.Gly5370Arg
XM_017009969.2:c.16288G>C	XP_016865458.1:p.Gly5430Arg
XM_017009972.1:c.9406G>C	XP_016865461.1:p.Gly3136Arg
XM_017009973.1:c.9385G>C	XP_016865462.1:p.Gly3129Arg
NR_003149.2:n.16283G>C