Canonical Allele Identifier: CA360425564

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119305G>T (hg19) ; chr5:g.90823488G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823488G>T , CM000667.2:g.90823488G>T	GRCh38
NC_000005.9:g.90119305G>T , CM000667.1:g.90119305G>T	GRCh37
NC_000005.8:g.90155061G>T	NCBI36
NG_007083.1:g.269689G>T
NG_007083.2:g.299145G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.16260G>T MANE Select	ENSP00000384582.2:p.Gln5420His
ENST00000425867.3:c.5214G>T	ENSP00000392618.3:p.Gln1738His
ENST00000638510.1:n.3527G>T
ENST00000639431.1:c.265+147279G>T	ENSP00000491057.1:n.265+147279G>T
ENST00000640061.1:n.128+1306G>T
ENST00000640407.1:c.2670G>T	ENSP00000491425.1:p.Gln890His
ENST00000405460.6:c.16260G>T	ENSP00000384582.2:p.Gln5420His
ENST00000425867.2:c.3243G>T	ENSP00000392618.2:p.Gln1081His
NM_032119.3:c.16260G>T	NP_115495.3:p.Gln5420His
NR_003149.1:n.16273G>T
XM_011543675.1:c.16257G>T	XP_011541977.1:p.Gln5419His
XM_011543676.1:c.16179G>T	XP_011541978.1:p.Gln5393His
XM_011543677.1:c.13563G>T	XP_011541979.1:p.Gln4521His
NM_032119.4:c.16260G>T MANE Select	NP_115495.3:p.Gln5420His
XM_017009963.2:c.16281G>T	XP_016865452.1:p.Gln5427His
XM_017009964.2:c.16278G>T	XP_016865453.1:p.Gln5426His
XM_017009965.1:c.16278G>T	XP_016865454.1:p.Gln5426His
XM_017009966.2:c.16200G>T	XP_016865455.1:p.Gln5400His
XM_017009967.1:c.16185G>T	XP_016865456.1:p.Gln5395His
XM_017009968.2:c.16101G>T	XP_016865457.1:p.Gln5367His
XM_017009969.2:c.16281G>T	XP_016865458.1:p.Gln5427His
XM_017009972.1:c.9399G>T	XP_016865461.1:p.Gln3133His
XM_017009973.1:c.9378G>T	XP_016865462.1:p.Gln3126His
NR_003149.2:n.16276G>T