Canonical Allele Identifier: CA445406412

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90763340-T-C
• MyVariant Identifiers: chr5:g.90059157T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763340T>C , CM000667.2:g.90763340T>C	GRCh38
NC_000005.9:g.90059157T>C , CM000667.1:g.90059157T>C	GRCh37
NC_000005.8:g.90094913T>C	NCBI36
NG_007083.1:g.209541T>C
NG_007083.2:g.238997T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12156T>C MANE Select	ENSP00000384582.2:p.Pro4052=
ENST00000425867.3:c.1110T>C	ENSP00000392618.3:p.Pro370=
ENST00000639431.1:c.265+87131T>C	ENSP00000491057.1:n.265+87131T>C
ENST00000640464.1:n.2575T>C
ENST00000640729.1:n.733T>C
ENST00000405460.6:c.12156T>C	ENSP00000384582.2:p.Pro4052=
NM_032119.3:c.12156T>C	NP_115495.3:p.Pro4052=
NR_003149.1:n.12169T>C
XM_011543675.1:c.12153T>C	XP_011541977.1:p.Pro4051=
XM_011543676.1:c.12075T>C	XP_011541978.1:p.Pro4025=
XM_011543677.1:c.9459T>C	XP_011541979.1:p.Pro3153=
XM_011543678.1:c.12156T>C	XP_011541980.1:p.Pro4052=
NM_032119.4:c.12156T>C MANE Select	NP_115495.3:p.Pro4052=
XM_017009963.2:c.12177T>C	XP_016865452.1:p.Pro4059=
XM_017009964.2:c.12174T>C	XP_016865453.1:p.Pro4058=
XM_017009965.1:c.12174T>C	XP_016865454.1:p.Pro4058=
XM_017009966.2:c.12096T>C	XP_016865455.1:p.Pro4032=
XM_017009967.1:c.12081T>C	XP_016865456.1:p.Pro4027=
XM_017009968.2:c.12177T>C	XP_016865457.1:p.Pro4059=
XM_017009969.2:c.12177T>C	XP_016865458.1:p.Pro4059=
XM_017009970.2:c.12177T>C	XP_016865459.1:p.Pro4059=
XM_017009971.2:c.12177T>C	XP_016865460.1:p.Pro4059=
XM_017009972.1:c.5295T>C	XP_016865461.1:p.Pro1765=
XM_017009973.1:c.5274T>C	XP_016865462.1:p.Pro1758=
NR_003149.2:n.12172T>C