Canonical Allele Identifier: CA360410373

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106723A>C (hg19) ; chr5:g.90810906A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810906A>C , CM000667.2:g.90810906A>C	GRCh38
NC_000005.9:g.90106723A>C , CM000667.1:g.90106723A>C	GRCh37
NC_000005.8:g.90142479A>C	NCBI36
NG_007083.1:g.257107A>C
NG_007083.2:g.286563A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15646A>C MANE Select	ENSP00000384582.2:p.Ile5216Leu
ENST00000425867.3:c.4600A>C	ENSP00000392618.3:p.Ile1534Leu
ENST00000638510.1:n.2913A>C
ENST00000639431.1:c.265+134697A>C	ENSP00000491057.1:n.265+134697A>C
ENST00000640407.1:c.2056A>C	ENSP00000491425.1:p.Ile686Leu
ENST00000405460.6:c.15646A>C	ENSP00000384582.2:p.Ile5216Leu
ENST00000425867.2:c.2629A>C	ENSP00000392618.2:p.Ile877Leu
NM_032119.3:c.15646A>C	NP_115495.3:p.Ile5216Leu
NR_003149.1:n.15659A>C
XM_011543675.1:c.15643A>C	XP_011541977.1:p.Ile5215Leu
XM_011543676.1:c.15565A>C	XP_011541978.1:p.Ile5189Leu
XM_011543677.1:c.12949A>C	XP_011541979.1:p.Ile4317Leu
NM_032119.4:c.15646A>C MANE Select	NP_115495.3:p.Ile5216Leu
XM_017009963.2:c.15667A>C	XP_016865452.1:p.Ile5223Leu
XM_017009964.2:c.15664A>C	XP_016865453.1:p.Ile5222Leu
XM_017009965.1:c.15664A>C	XP_016865454.1:p.Ile5222Leu
XM_017009966.2:c.15586A>C	XP_016865455.1:p.Ile5196Leu
XM_017009967.1:c.15571A>C	XP_016865456.1:p.Ile5191Leu
XM_017009968.2:c.15487A>C	XP_016865457.1:p.Ile5163Leu
XM_017009969.2:c.15667A>C	XP_016865458.1:p.Ile5223Leu
XM_017009972.1:c.8785A>C	XP_016865461.1:p.Ile2929Leu
XM_017009973.1:c.8764A>C	XP_016865462.1:p.Ile2922Leu
NR_003149.2:n.15662A>C