Canonical Allele Identifier: CA360425614

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119331A>C (hg19) ; chr5:g.90823514A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823514A>C , CM000667.2:g.90823514A>C	GRCh38
NC_000005.9:g.90119331A>C , CM000667.1:g.90119331A>C	GRCh37
NC_000005.8:g.90155087A>C	NCBI36
NG_007083.1:g.269715A>C
NG_007083.2:g.299171A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16286A>C MANE Select	ENSP00000384582.2:p.Glu5429Ala
ENST00000425867.3:c.5240A>C	ENSP00000392618.3:p.Glu1747Ala
ENST00000638510.1:n.3553A>C
ENST00000639431.1:c.265+147305A>C	ENSP00000491057.1:n.265+147305A>C
ENST00000640061.1:n.128+1332A>C
ENST00000640407.1:c.2696A>C	ENSP00000491425.1:p.Glu899Ala
ENST00000405460.6:c.16286A>C	ENSP00000384582.2:p.Glu5429Ala
ENST00000425867.2:c.3269A>C	ENSP00000392618.2:p.Glu1090Ala
NM_032119.3:c.16286A>C	NP_115495.3:p.Glu5429Ala
NR_003149.1:n.16299A>C
XM_011543675.1:c.16283A>C	XP_011541977.1:p.Glu5428Ala
XM_011543676.1:c.16205A>C	XP_011541978.1:p.Glu5402Ala
XM_011543677.1:c.13589A>C	XP_011541979.1:p.Glu4530Ala
NM_032119.4:c.16286A>C MANE Select	NP_115495.3:p.Glu5429Ala
XM_017009963.2:c.16307A>C	XP_016865452.1:p.Glu5436Ala
XM_017009964.2:c.16304A>C	XP_016865453.1:p.Glu5435Ala
XM_017009965.1:c.16304A>C	XP_016865454.1:p.Glu5435Ala
XM_017009966.2:c.16226A>C	XP_016865455.1:p.Glu5409Ala
XM_017009967.1:c.16211A>C	XP_016865456.1:p.Glu5404Ala
XM_017009968.2:c.16127A>C	XP_016865457.1:p.Glu5376Ala
XM_017009969.2:c.16307A>C	XP_016865458.1:p.Glu5436Ala
XM_017009972.1:c.9425A>C	XP_016865461.1:p.Glu3142Ala
XM_017009973.1:c.9404A>C	XP_016865462.1:p.Glu3135Ala
NR_003149.2:n.16302A>C