Canonical Allele Identifier: CA360425559

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119303C>T (hg19) ; chr5:g.90823486C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823486C>T , CM000667.2:g.90823486C>T	GRCh38
NC_000005.9:g.90119303C>T , CM000667.1:g.90119303C>T	GRCh37
NC_000005.8:g.90155059C>T	NCBI36
NG_007083.1:g.269687C>T
NG_007083.2:g.299143C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16258C>T MANE Select	ENSP00000384582.2:p.Gln5420Ter
ENST00000425867.3:c.5212C>T	ENSP00000392618.3:p.Gln1738Ter
ENST00000638510.1:n.3525C>T
ENST00000639431.1:c.265+147277C>T	ENSP00000491057.1:n.265+147277C>T
ENST00000640061.1:n.128+1304C>T
ENST00000640407.1:c.2668C>T	ENSP00000491425.1:p.Gln890Ter
ENST00000405460.6:c.16258C>T	ENSP00000384582.2:p.Gln5420Ter
ENST00000425867.2:c.3241C>T	ENSP00000392618.2:p.Gln1081Ter
NM_032119.3:c.16258C>T	NP_115495.3:p.Gln5420Ter
NR_003149.1:n.16271C>T
XM_011543675.1:c.16255C>T	XP_011541977.1:p.Gln5419Ter
XM_011543676.1:c.16177C>T	XP_011541978.1:p.Gln5393Ter
XM_011543677.1:c.13561C>T	XP_011541979.1:p.Gln4521Ter
NM_032119.4:c.16258C>T MANE Select	NP_115495.3:p.Gln5420Ter
XM_017009963.2:c.16279C>T	XP_016865452.1:p.Gln5427Ter
XM_017009964.2:c.16276C>T	XP_016865453.1:p.Gln5426Ter
XM_017009965.1:c.16276C>T	XP_016865454.1:p.Gln5426Ter
XM_017009966.2:c.16198C>T	XP_016865455.1:p.Gln5400Ter
XM_017009967.1:c.16183C>T	XP_016865456.1:p.Gln5395Ter
XM_017009968.2:c.16099C>T	XP_016865457.1:p.Gln5367Ter
XM_017009969.2:c.16279C>T	XP_016865458.1:p.Gln5427Ter
XM_017009972.1:c.9397C>T	XP_016865461.1:p.Gln3133Ter
XM_017009973.1:c.9376C>T	XP_016865462.1:p.Gln3126Ter
NR_003149.2:n.16274C>T