Canonical Allele Identifier: CA360403196

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1751660055
• MyVariant Identifiers: chr5:g.90021382T>C (hg19) ; chr5:g.90725565T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725565T>C , CM000667.2:g.90725565T>C	GRCh38
NC_000005.9:g.90021382T>C , CM000667.1:g.90021382T>C	GRCh37
NC_000005.8:g.90057138T>C	NCBI36
NG_007083.1:g.171766T>C
NG_007083.2:g.201222T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10070T>C MANE Select	ENSP00000384582.2:p.Ile3357Thr
ENST00000639431.1:c.265+49356T>C	ENSP00000491057.1:n.265+49356T>C
ENST00000640374.1:n.3214T>C
ENST00000640464.1:n.489T>C
ENST00000405460.6:c.10070T>C	ENSP00000384582.2:p.Ile3357Thr
ENST00000509621.1:c.2767T>C
NM_032119.3:c.10070T>C	NP_115495.3:p.Ile3357Thr
NR_003149.1:n.10083T>C
XM_011543675.1:c.10067T>C	XP_011541977.1:p.Ile3356Thr
XM_011543676.1:c.9989T>C	XP_011541978.1:p.Ile3330Thr
XM_011543677.1:c.7373T>C	XP_011541979.1:p.Ile2458Thr
XM_011543678.1:c.10070T>C	XP_011541980.1:p.Ile3357Thr
XM_011543679.1:c.10070T>C	XP_011541981.1:p.Ile3357Thr
XR_948560.1:n.272-9756A>G
NM_032119.4:c.10070T>C MANE Select	NP_115495.3:p.Ile3357Thr
XM_017009963.2:c.10091T>C	XP_016865452.1:p.Ile3364Thr
XM_017009964.2:c.10088T>C	XP_016865453.1:p.Ile3363Thr
XM_017009965.1:c.10088T>C	XP_016865454.1:p.Ile3363Thr
XM_017009966.2:c.10010T>C	XP_016865455.1:p.Ile3337Thr
XM_017009967.1:c.9995T>C	XP_016865456.1:p.Ile3332Thr
XM_017009968.2:c.10091T>C	XP_016865457.1:p.Ile3364Thr
XM_017009969.2:c.10091T>C	XP_016865458.1:p.Ile3364Thr
XM_017009970.2:c.10091T>C	XP_016865459.1:p.Ile3364Thr
XM_017009971.2:c.10091T>C	XP_016865460.1:p.Ile3364Thr
XM_017009972.1:c.3209T>C	XP_016865461.1:p.Ile1070Thr
XM_017009973.1:c.3188T>C	XP_016865462.1:p.Ile1063Thr
XM_017009974.2:c.10091T>C	XP_016865463.1:p.Ile3364Thr
XR_001742802.1:n.2523-9756A>G
NR_003149.2:n.10086T>C