Canonical Allele Identifier: CA445404567

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90692745-T-C
• MyVariant Identifiers: chr5:g.89988562T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692745T>C , CM000667.2:g.90692745T>C	GRCh38
NC_000005.9:g.89988562T>C , CM000667.1:g.89988562T>C	GRCh37
NC_000005.8:g.90024318T>C	NCBI36
NG_007083.1:g.138946T>C
NG_007083.2:g.168402T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.7092T>C MANE Select	ENSP00000384582.2:p.Pro2364=
ENST00000639431.1:c.265+16536T>C	ENSP00000491057.1:n.265+16536T>C
ENST00000639473.1:n.2551T>C
ENST00000640012.1:c.899T>C
ENST00000640374.1:n.236T>C
ENST00000640403.1:c.4383T>C	ENSP00000492531.1:p.Pro1461=
ENST00000640779.1:c.1821T>C
ENST00000405460.6:c.7092T>C	ENSP00000384582.2:p.Pro2364=
NM_032119.3:c.7092T>C	NP_115495.3:p.Pro2364=
NR_003149.1:n.7105T>C
XM_011543675.1:c.7089T>C	XP_011541977.1:p.Pro2363=
XM_011543676.1:c.7011T>C	XP_011541978.1:p.Pro2337=
XM_011543677.1:c.4395T>C	XP_011541979.1:p.Pro1465=
XM_011543678.1:c.7092T>C	XP_011541980.1:p.Pro2364=
XM_011543679.1:c.7092T>C	XP_011541981.1:p.Pro2364=
NM_032119.4:c.7092T>C MANE Select	NP_115495.3:p.Pro2364=
XM_017009963.2:c.7092T>C	XP_016865452.1:p.Pro2364=
XM_017009964.2:c.7089T>C	XP_016865453.1:p.Pro2363=
XM_017009965.1:c.7089T>C	XP_016865454.1:p.Pro2363=
XM_017009966.2:c.7011T>C	XP_016865455.1:p.Pro2337=
XM_017009967.1:c.6996T>C	XP_016865456.1:p.Pro2332=
XM_017009968.2:c.7092T>C	XP_016865457.1:p.Pro2364=
XM_017009969.2:c.7092T>C	XP_016865458.1:p.Pro2364=
XM_017009970.2:c.7092T>C	XP_016865459.1:p.Pro2364=
XM_017009971.2:c.7092T>C	XP_016865460.1:p.Pro2364=
XM_017009972.1:c.210T>C	XP_016865461.1:p.Pro70=
XM_017009973.1:c.210T>C	XP_016865462.1:p.Pro70=
XM_017009974.2:c.7092T>C	XP_016865463.1:p.Pro2364=
NR_003149.2:n.7108T>C