Canonical Allele Identifier: CA360366985

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1561663986
• gnomAD v4: 5-90755111-T-C
• MyVariant Identifiers: chr5:g.90050928T>C (hg19) ; chr5:g.90755111T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755111T>C , CM000667.2:g.90755111T>C	GRCh38
NC_000005.9:g.90050928T>C , CM000667.1:g.90050928T>C	GRCh37
NC_000005.8:g.90086684T>C	NCBI36
NG_007083.1:g.201312T>C
NG_007083.2:g.230768T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11506T>C MANE Select	ENSP00000384582.2:p.Tyr3836His
ENST00000425867.3:c.637T>C	ENSP00000392618.3:p.Tyr213His
ENST00000639431.1:c.265+78902T>C	ENSP00000491057.1:n.265+78902T>C
ENST00000640374.1:n.4650T>C
ENST00000640464.1:n.1925T>C
ENST00000405460.6:c.11506T>C	ENSP00000384582.2:p.Tyr3836His
ENST00000509621.1:c.4203T>C
NM_032119.3:c.11506T>C	NP_115495.3:p.Tyr3836His
NR_003149.1:n.11519T>C
XM_011543675.1:c.11503T>C	XP_011541977.1:p.Tyr3835His
XM_011543676.1:c.11425T>C	XP_011541978.1:p.Tyr3809His
XM_011543677.1:c.8809T>C	XP_011541979.1:p.Tyr2937His
XM_011543678.1:c.11506T>C	XP_011541980.1:p.Tyr3836His
NM_032119.4:c.11506T>C MANE Select	NP_115495.3:p.Tyr3836His
XM_017009963.2:c.11527T>C	XP_016865452.1:p.Tyr3843His
XM_017009964.2:c.11524T>C	XP_016865453.1:p.Tyr3842His
XM_017009965.1:c.11524T>C	XP_016865454.1:p.Tyr3842His
XM_017009966.2:c.11446T>C	XP_016865455.1:p.Tyr3816His
XM_017009967.1:c.11431T>C	XP_016865456.1:p.Tyr3811His
XM_017009968.2:c.11527T>C	XP_016865457.1:p.Tyr3843His
XM_017009969.2:c.11527T>C	XP_016865458.1:p.Tyr3843His
XM_017009970.2:c.11527T>C	XP_016865459.1:p.Tyr3843His
XM_017009971.2:c.11527T>C	XP_016865460.1:p.Tyr3843His
XM_017009972.1:c.4645T>C	XP_016865461.1:p.Tyr1549His
XM_017009973.1:c.4624T>C	XP_016865462.1:p.Tyr1542His
NR_003149.2:n.11522T>C