Canonical Allele Identifier: CA445415803

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90789767-T-C
• MyVariant Identifiers: chr5:g.90085584T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789767T>C , CM000667.2:g.90789767T>C	GRCh38
NC_000005.9:g.90085584T>C , CM000667.1:g.90085584T>C	GRCh37
NC_000005.8:g.90121340T>C	NCBI36
NG_007083.1:g.235968T>C
NG_007083.2:g.265424T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.13959T>C MANE Select	ENSP00000384582.2:p.Thr4653=
ENST00000425867.3:c.2913T>C	ENSP00000392618.3:p.Thr971=
ENST00000638510.1:n.1226T>C
ENST00000638975.1:c.588T>C	ENSP00000492630.1:p.Thr196=
ENST00000639431.1:c.265+113558T>C	ENSP00000491057.1:n.265+113558T>C
ENST00000640407.1:c.369T>C	ENSP00000491425.1:p.Thr123=
ENST00000405460.6:c.13959T>C	ENSP00000384582.2:p.Thr4653=
ENST00000425867.2:c.942T>C	ENSP00000392618.2:p.Thr314=
NM_032119.3:c.13959T>C	NP_115495.3:p.Thr4653=
NR_003149.1:n.13972T>C
XM_011543675.1:c.13956T>C	XP_011541977.1:p.Thr4652=
XM_011543676.1:c.13878T>C	XP_011541978.1:p.Thr4626=
XM_011543677.1:c.11262T>C	XP_011541979.1:p.Thr3754=
XM_011543678.1:c.13959T>C	XP_011541980.1:p.Thr4653=
NM_032119.4:c.13959T>C MANE Select	NP_115495.3:p.Thr4653=
XM_017009963.2:c.13980T>C	XP_016865452.1:p.Thr4660=
XM_017009964.2:c.13977T>C	XP_016865453.1:p.Thr4659=
XM_017009965.1:c.13977T>C	XP_016865454.1:p.Thr4659=
XM_017009966.2:c.13899T>C	XP_016865455.1:p.Thr4633=
XM_017009967.1:c.13884T>C	XP_016865456.1:p.Thr4628=
XM_017009968.2:c.13980T>C	XP_016865457.1:p.Thr4660=
XM_017009969.2:c.13980T>C	XP_016865458.1:p.Thr4660=
XM_017009970.2:c.13980T>C	XP_016865459.1:p.Thr4660=
XM_017009971.2:c.13980T>C	XP_016865460.1:p.Thr4660=
XM_017009972.1:c.7098T>C	XP_016865461.1:p.Thr2366=
XM_017009973.1:c.7077T>C	XP_016865462.1:p.Thr2359=
NR_003149.2:n.13975T>C