Canonical Allele Identifier: CA360425573

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119309G>C (hg19) ; chr5:g.90823492G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823492G>C , CM000667.2:g.90823492G>C	GRCh38
NC_000005.9:g.90119309G>C , CM000667.1:g.90119309G>C	GRCh37
NC_000005.8:g.90155065G>C	NCBI36
NG_007083.1:g.269693G>C
NG_007083.2:g.299149G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16264G>C MANE Select	ENSP00000384582.2:p.Asp5422His
ENST00000425867.3:c.5218G>C	ENSP00000392618.3:p.Asp1740His
ENST00000638510.1:n.3531G>C
ENST00000639431.1:c.265+147283G>C	ENSP00000491057.1:n.265+147283G>C
ENST00000640061.1:n.128+1310G>C
ENST00000640407.1:c.2674G>C	ENSP00000491425.1:p.Asp892His
ENST00000405460.6:c.16264G>C	ENSP00000384582.2:p.Asp5422His
ENST00000425867.2:c.3247G>C	ENSP00000392618.2:p.Asp1083His
NM_032119.3:c.16264G>C	NP_115495.3:p.Asp5422His
NR_003149.1:n.16277G>C
XM_011543675.1:c.16261G>C	XP_011541977.1:p.Asp5421His
XM_011543676.1:c.16183G>C	XP_011541978.1:p.Asp5395His
XM_011543677.1:c.13567G>C	XP_011541979.1:p.Asp4523His
NM_032119.4:c.16264G>C MANE Select	NP_115495.3:p.Asp5422His
XM_017009963.2:c.16285G>C	XP_016865452.1:p.Asp5429His
XM_017009964.2:c.16282G>C	XP_016865453.1:p.Asp5428His
XM_017009965.1:c.16282G>C	XP_016865454.1:p.Asp5428His
XM_017009966.2:c.16204G>C	XP_016865455.1:p.Asp5402His
XM_017009967.1:c.16189G>C	XP_016865456.1:p.Asp5397His
XM_017009968.2:c.16105G>C	XP_016865457.1:p.Asp5369His
XM_017009969.2:c.16285G>C	XP_016865458.1:p.Asp5429His
XM_017009972.1:c.9403G>C	XP_016865461.1:p.Asp3135His
XM_017009973.1:c.9382G>C	XP_016865462.1:p.Asp3128His
NR_003149.2:n.16280G>C