Canonical Allele Identifier: CA445404093

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90755080-T-C
• MyVariant Identifiers: chr5:g.90050897T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755080T>C , CM000667.2:g.90755080T>C	GRCh38
NC_000005.9:g.90050897T>C , CM000667.1:g.90050897T>C	GRCh37
NC_000005.8:g.90086653T>C	NCBI36
NG_007083.1:g.201281T>C
NG_007083.2:g.230737T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11475T>C MANE Select	ENSP00000384582.2:p.His3825=
ENST00000425867.3:c.606T>C	ENSP00000392618.3:p.His202=
ENST00000639431.1:c.265+78871T>C	ENSP00000491057.1:n.265+78871T>C
ENST00000640374.1:n.4619T>C
ENST00000640464.1:n.1894T>C
ENST00000405460.6:c.11475T>C	ENSP00000384582.2:p.His3825=
ENST00000509621.1:c.4172T>C
NM_032119.3:c.11475T>C	NP_115495.3:p.His3825=
NR_003149.1:n.11488T>C
XM_011543675.1:c.11472T>C	XP_011541977.1:p.His3824=
XM_011543676.1:c.11394T>C	XP_011541978.1:p.His3798=
XM_011543677.1:c.8778T>C	XP_011541979.1:p.His2926=
XM_011543678.1:c.11475T>C	XP_011541980.1:p.His3825=
NM_032119.4:c.11475T>C MANE Select	NP_115495.3:p.His3825=
XM_017009963.2:c.11496T>C	XP_016865452.1:p.His3832=
XM_017009964.2:c.11493T>C	XP_016865453.1:p.His3831=
XM_017009965.1:c.11493T>C	XP_016865454.1:p.His3831=
XM_017009966.2:c.11415T>C	XP_016865455.1:p.His3805=
XM_017009967.1:c.11400T>C	XP_016865456.1:p.His3800=
XM_017009968.2:c.11496T>C	XP_016865457.1:p.His3832=
XM_017009969.2:c.11496T>C	XP_016865458.1:p.His3832=
XM_017009970.2:c.11496T>C	XP_016865459.1:p.His3832=
XM_017009971.2:c.11496T>C	XP_016865460.1:p.His3832=
XM_017009972.1:c.4614T>C	XP_016865461.1:p.His1538=
XM_017009973.1:c.4593T>C	XP_016865462.1:p.His1531=
NR_003149.2:n.11491T>C