Canonical Allele Identifier: CA360409134

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041494A>C (hg19) ; chr5:g.90745677A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745677A>C , CM000667.2:g.90745677A>C	GRCh38
NC_000005.9:g.90041494A>C , CM000667.1:g.90041494A>C	GRCh37
NC_000005.8:g.90077250A>C	NCBI36
NG_007083.1:g.191878A>C
NG_007083.2:g.221334A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10856A>C MANE Select	ENSP00000384582.2:p.Glu3619Ala
ENST00000639431.1:c.265+69468A>C	ENSP00000491057.1:n.265+69468A>C
ENST00000640374.1:n.4000A>C
ENST00000640464.1:n.1275A>C
ENST00000405460.6:c.10856A>C	ENSP00000384582.2:p.Glu3619Ala
ENST00000509621.1:c.3553A>C
NM_032119.3:c.10856A>C	NP_115495.3:p.Glu3619Ala
NR_003149.1:n.10869A>C
XM_011543675.1:c.10853A>C	XP_011541977.1:p.Glu3618Ala
XM_011543676.1:c.10775A>C	XP_011541978.1:p.Glu3592Ala
XM_011543677.1:c.8159A>C	XP_011541979.1:p.Glu2720Ala
XM_011543678.1:c.10856A>C	XP_011541980.1:p.Glu3619Ala
XM_011543679.1:c.*78A>C	XP_011541981.1:n.*78A>C
NM_032119.4:c.10856A>C MANE Select	NP_115495.3:p.Glu3619Ala
XM_017009963.2:c.10877A>C	XP_016865452.1:p.Glu3626Ala
XM_017009964.2:c.10874A>C	XP_016865453.1:p.Glu3625Ala
XM_017009965.1:c.10874A>C	XP_016865454.1:p.Glu3625Ala
XM_017009966.2:c.10796A>C	XP_016865455.1:p.Glu3599Ala
XM_017009967.1:c.10781A>C	XP_016865456.1:p.Glu3594Ala
XM_017009968.2:c.10877A>C	XP_016865457.1:p.Glu3626Ala
XM_017009969.2:c.10877A>C	XP_016865458.1:p.Glu3626Ala
XM_017009970.2:c.10877A>C	XP_016865459.1:p.Glu3626Ala
XM_017009971.2:c.10877A>C	XP_016865460.1:p.Glu3626Ala
XM_017009972.1:c.3995A>C	XP_016865461.1:p.Glu1332Ala
XM_017009973.1:c.3974A>C	XP_016865462.1:p.Glu1325Ala
XM_017009974.2:c.*78A>C	XP_016865463.1:n.*78A>C
NR_003149.2:n.10872A>C