Canonical Allele Identifier: CA360397235

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012377A>C (hg19) ; chr5:g.90716560A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716560A>C , CM000667.2:g.90716560A>C	GRCh38
NC_000005.9:g.90012377A>C , CM000667.1:g.90012377A>C	GRCh37
NC_000005.8:g.90048133A>C	NCBI36
NG_007083.1:g.162761A>C
NG_007083.2:g.192217A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9278A>C MANE Select	ENSP00000384582.2:p.Tyr3093Ser
ENST00000639431.1:c.265+40351A>C	ENSP00000491057.1:n.265+40351A>C
ENST00000639473.1:n.4737A>C
ENST00000640012.1:c.3085A>C
ENST00000640374.1:n.2422A>C
ENST00000640779.1:c.4007A>C
ENST00000405460.6:c.9278A>C	ENSP00000384582.2:p.Tyr3093Ser
ENST00000509621.1:c.1975A>C
NM_032119.3:c.9278A>C	NP_115495.3:p.Tyr3093Ser
NR_003149.1:n.9291A>C
XM_011543675.1:c.9275A>C	XP_011541977.1:p.Tyr3092Ser
XM_011543676.1:c.9197A>C	XP_011541978.1:p.Tyr3066Ser
XM_011543677.1:c.6581A>C	XP_011541979.1:p.Tyr2194Ser
XM_011543678.1:c.9278A>C	XP_011541980.1:p.Tyr3093Ser
XM_011543679.1:c.9278A>C	XP_011541981.1:p.Tyr3093Ser
XR_948560.1:n.272-751T>G
NM_032119.4:c.9278A>C MANE Select	NP_115495.3:p.Tyr3093Ser
XM_017009963.2:c.9299A>C	XP_016865452.1:p.Tyr3100Ser
XM_017009964.2:c.9296A>C	XP_016865453.1:p.Tyr3099Ser
XM_017009965.1:c.9296A>C	XP_016865454.1:p.Tyr3099Ser
XM_017009966.2:c.9218A>C	XP_016865455.1:p.Tyr3073Ser
XM_017009967.1:c.9203A>C	XP_016865456.1:p.Tyr3068Ser
XM_017009968.2:c.9299A>C	XP_016865457.1:p.Tyr3100Ser
XM_017009969.2:c.9299A>C	XP_016865458.1:p.Tyr3100Ser
XM_017009970.2:c.9299A>C	XP_016865459.1:p.Tyr3100Ser
XM_017009971.2:c.9299A>C	XP_016865460.1:p.Tyr3100Ser
XM_017009972.1:c.2417A>C	XP_016865461.1:p.Tyr806Ser
XM_017009973.1:c.2396A>C	XP_016865462.1:p.Tyr799Ser
XM_017009974.2:c.9299A>C	XP_016865463.1:p.Tyr3100Ser
XR_001742802.1:n.2523-751T>G
NR_003149.2:n.9294A>C