Canonical Allele Identifier: CA445414772

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90725563-T-C
• MyVariant Identifiers: chr5:g.90021380T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725563T>C , CM000667.2:g.90725563T>C	GRCh38
NC_000005.9:g.90021380T>C , CM000667.1:g.90021380T>C	GRCh37
NC_000005.8:g.90057136T>C	NCBI36
NG_007083.1:g.171764T>C
NG_007083.2:g.201220T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10068T>C MANE Select	ENSP00000384582.2:p.Ile3356=
ENST00000639431.1:c.265+49354T>C	ENSP00000491057.1:n.265+49354T>C
ENST00000640374.1:n.3212T>C
ENST00000640464.1:n.487T>C
ENST00000405460.6:c.10068T>C	ENSP00000384582.2:p.Ile3356=
ENST00000509621.1:c.2765T>C
NM_032119.3:c.10068T>C	NP_115495.3:p.Ile3356=
NR_003149.1:n.10081T>C
XM_011543675.1:c.10065T>C	XP_011541977.1:p.Ile3355=
XM_011543676.1:c.9987T>C	XP_011541978.1:p.Ile3329=
XM_011543677.1:c.7371T>C	XP_011541979.1:p.Ile2457=
XM_011543678.1:c.10068T>C	XP_011541980.1:p.Ile3356=
XM_011543679.1:c.10068T>C	XP_011541981.1:p.Ile3356=
XR_948560.1:n.272-9754A>G
NM_032119.4:c.10068T>C MANE Select	NP_115495.3:p.Ile3356=
XM_017009963.2:c.10089T>C	XP_016865452.1:p.Ile3363=
XM_017009964.2:c.10086T>C	XP_016865453.1:p.Ile3362=
XM_017009965.1:c.10086T>C	XP_016865454.1:p.Ile3362=
XM_017009966.2:c.10008T>C	XP_016865455.1:p.Ile3336=
XM_017009967.1:c.9993T>C	XP_016865456.1:p.Ile3331=
XM_017009968.2:c.10089T>C	XP_016865457.1:p.Ile3363=
XM_017009969.2:c.10089T>C	XP_016865458.1:p.Ile3363=
XM_017009970.2:c.10089T>C	XP_016865459.1:p.Ile3363=
XM_017009971.2:c.10089T>C	XP_016865460.1:p.Ile3363=
XM_017009972.1:c.3207T>C	XP_016865461.1:p.Ile1069=
XM_017009973.1:c.3186T>C	XP_016865462.1:p.Ile1062=
XM_017009974.2:c.10089T>C	XP_016865463.1:p.Ile3363=
XR_001742802.1:n.2523-9754A>G
NR_003149.2:n.10084T>C