Canonical Allele Identifier: CA360396122

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712291-T-C
• MyVariant Identifiers: chr5:g.90008108T>C (hg19) ; chr5:g.90712291T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712291T>C , CM000667.2:g.90712291T>C	GRCh38
NC_000005.9:g.90008108T>C , CM000667.1:g.90008108T>C	GRCh37
NC_000005.8:g.90043864T>C	NCBI36
NG_007083.1:g.158492T>C
NG_007083.2:g.187948T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9047T>C MANE Select	ENSP00000384582.2:p.Leu3016Pro
ENST00000639431.1:c.265+36082T>C	ENSP00000491057.1:n.265+36082T>C
ENST00000639473.1:n.4506T>C
ENST00000640012.1:c.2854T>C
ENST00000640374.1:n.2191T>C
ENST00000640779.1:c.3776T>C
ENST00000405460.6:c.9047T>C	ENSP00000384582.2:p.Leu3016Pro
ENST00000509621.1:c.1744T>C
NM_032119.3:c.9047T>C	NP_115495.3:p.Leu3016Pro
NR_003149.1:n.9060T>C
XM_011543675.1:c.9044T>C	XP_011541977.1:p.Leu3015Pro
XM_011543676.1:c.8966T>C	XP_011541978.1:p.Leu2989Pro
XM_011543677.1:c.6350T>C	XP_011541979.1:p.Leu2117Pro
XM_011543678.1:c.9047T>C	XP_011541980.1:p.Leu3016Pro
XM_011543679.1:c.9047T>C	XP_011541981.1:p.Leu3016Pro
NM_032119.4:c.9047T>C MANE Select	NP_115495.3:p.Leu3016Pro
XM_017009963.2:c.9068T>C	XP_016865452.1:p.Leu3023Pro
XM_017009964.2:c.9065T>C	XP_016865453.1:p.Leu3022Pro
XM_017009965.1:c.9065T>C	XP_016865454.1:p.Leu3022Pro
XM_017009966.2:c.8987T>C	XP_016865455.1:p.Leu2996Pro
XM_017009967.1:c.8972T>C	XP_016865456.1:p.Leu2991Pro
XM_017009968.2:c.9068T>C	XP_016865457.1:p.Leu3023Pro
XM_017009969.2:c.9068T>C	XP_016865458.1:p.Leu3023Pro
XM_017009970.2:c.9068T>C	XP_016865459.1:p.Leu3023Pro
XM_017009971.2:c.9068T>C	XP_016865460.1:p.Leu3023Pro
XM_017009972.1:c.2186T>C	XP_016865461.1:p.Leu729Pro
XM_017009973.1:c.2165T>C	XP_016865462.1:p.Leu722Pro
XM_017009974.2:c.9068T>C	XP_016865463.1:p.Leu3023Pro
NR_003149.2:n.9063T>C