Canonical Allele Identifier: CA445467615

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90087028T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791211T>C , CM000667.2:g.90791211T>C	GRCh38
NC_000005.9:g.90087028T>C , CM000667.1:g.90087028T>C	GRCh37
NC_000005.8:g.90122784T>C	NCBI36
NG_007083.1:g.237412T>C
NG_007083.2:g.266868T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14382T>C MANE Select	ENSP00000384582.2:p.Phe4794=
ENST00000425867.3:c.3336T>C	ENSP00000392618.3:p.Phe1112=
ENST00000507314.2:c.57T>C	ENSP00000491299.1:p.Phe19=
ENST00000638510.1:n.1649T>C
ENST00000638585.1:n.148T>C
ENST00000638975.1:c.1011T>C	ENSP00000492630.1:p.Phe337=
ENST00000639431.1:c.265+115002T>C	ENSP00000491057.1:n.265+115002T>C
ENST00000640407.1:c.792T>C	ENSP00000491425.1:p.Phe264=
ENST00000405460.6:c.14382T>C	ENSP00000384582.2:p.Phe4794=
ENST00000425867.2:c.1365T>C	ENSP00000392618.2:p.Phe455=
ENST00000507314.1:n.57T>C
NM_032119.3:c.14382T>C	NP_115495.3:p.Phe4794=
NR_003149.1:n.14395T>C
XM_011543675.1:c.14379T>C	XP_011541977.1:p.Phe4793=
XM_011543676.1:c.14301T>C	XP_011541978.1:p.Phe4767=
XM_011543677.1:c.11685T>C	XP_011541979.1:p.Phe3895=
XM_011543678.1:c.14382T>C	XP_011541980.1:p.Phe4794=
NM_032119.4:c.14382T>C MANE Select	NP_115495.3:p.Phe4794=
XM_017009963.2:c.14403T>C	XP_016865452.1:p.Phe4801=
XM_017009964.2:c.14400T>C	XP_016865453.1:p.Phe4800=
XM_017009965.1:c.14400T>C	XP_016865454.1:p.Phe4800=
XM_017009966.2:c.14322T>C	XP_016865455.1:p.Phe4774=
XM_017009967.1:c.14307T>C	XP_016865456.1:p.Phe4769=
XM_017009968.2:c.14403T>C	XP_016865457.1:p.Phe4801=
XM_017009969.2:c.14403T>C	XP_016865458.1:p.Phe4801=
XM_017009970.2:c.14403T>C	XP_016865459.1:p.Phe4801=
XM_017009971.2:c.14403T>C	XP_016865460.1:p.Phe4801=
XM_017009972.1:c.7521T>C	XP_016865461.1:p.Phe2507=
XM_017009973.1:c.7500T>C	XP_016865462.1:p.Phe2500=
NR_003149.2:n.14398T>C