Canonical Allele Identifier: CA360367460

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050995T>C (hg19) ; chr5:g.90755178T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755178T>C , CM000667.2:g.90755178T>C	GRCh38
NC_000005.9:g.90050995T>C , CM000667.1:g.90050995T>C	GRCh37
NC_000005.8:g.90086751T>C	NCBI36
NG_007083.1:g.201379T>C
NG_007083.2:g.230835T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11573T>C MANE Select	ENSP00000384582.2:p.Ile3858Thr
ENST00000425867.3:c.704T>C	ENSP00000392618.3:p.Ile235Thr
ENST00000639431.1:c.265+78969T>C	ENSP00000491057.1:n.265+78969T>C
ENST00000640374.1:n.4717T>C
ENST00000640464.1:n.1992T>C
ENST00000405460.6:c.11573T>C	ENSP00000384582.2:p.Ile3858Thr
ENST00000509621.1:c.4270T>C
NM_032119.3:c.11573T>C	NP_115495.3:p.Ile3858Thr
NR_003149.1:n.11586T>C
XM_011543675.1:c.11570T>C	XP_011541977.1:p.Ile3857Thr
XM_011543676.1:c.11492T>C	XP_011541978.1:p.Ile3831Thr
XM_011543677.1:c.8876T>C	XP_011541979.1:p.Ile2959Thr
XM_011543678.1:c.11573T>C	XP_011541980.1:p.Ile3858Thr
NM_032119.4:c.11573T>C MANE Select	NP_115495.3:p.Ile3858Thr
XM_017009963.2:c.11594T>C	XP_016865452.1:p.Ile3865Thr
XM_017009964.2:c.11591T>C	XP_016865453.1:p.Ile3864Thr
XM_017009965.1:c.11591T>C	XP_016865454.1:p.Ile3864Thr
XM_017009966.2:c.11513T>C	XP_016865455.1:p.Ile3838Thr
XM_017009967.1:c.11498T>C	XP_016865456.1:p.Ile3833Thr
XM_017009968.2:c.11594T>C	XP_016865457.1:p.Ile3865Thr
XM_017009969.2:c.11594T>C	XP_016865458.1:p.Ile3865Thr
XM_017009970.2:c.11594T>C	XP_016865459.1:p.Ile3865Thr
XM_017009971.2:c.11594T>C	XP_016865460.1:p.Ile3865Thr
XM_017009972.1:c.4712T>C	XP_016865461.1:p.Ile1571Thr
XM_017009973.1:c.4691T>C	XP_016865462.1:p.Ile1564Thr
NR_003149.2:n.11589T>C