Canonical Allele Identifier: CA445416090

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041474T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745657T>C , CM000667.2:g.90745657T>C	GRCh38
NC_000005.9:g.90041474T>C , CM000667.1:g.90041474T>C	GRCh37
NC_000005.8:g.90077230T>C	NCBI36
NG_007083.1:g.191858T>C
NG_007083.2:g.221314T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10836T>C MANE Select	ENSP00000384582.2:p.Asp3612=
ENST00000639431.1:c.265+69448T>C	ENSP00000491057.1:n.265+69448T>C
ENST00000640374.1:n.3980T>C
ENST00000640464.1:n.1255T>C
ENST00000405460.6:c.10836T>C	ENSP00000384582.2:p.Asp3612=
ENST00000509621.1:c.3533T>C
NM_032119.3:c.10836T>C	NP_115495.3:p.Asp3612=
NR_003149.1:n.10849T>C
XM_011543675.1:c.10833T>C	XP_011541977.1:p.Asp3611=
XM_011543676.1:c.10755T>C	XP_011541978.1:p.Asp3585=
XM_011543677.1:c.8139T>C	XP_011541979.1:p.Asp2713=
XM_011543678.1:c.10836T>C	XP_011541980.1:p.Asp3612=
XM_011543679.1:c.*58T>C	XP_011541981.1:n.*58T>C
NM_032119.4:c.10836T>C MANE Select	NP_115495.3:p.Asp3612=
XM_017009963.2:c.10857T>C	XP_016865452.1:p.Asp3619=
XM_017009964.2:c.10854T>C	XP_016865453.1:p.Asp3618=
XM_017009965.1:c.10854T>C	XP_016865454.1:p.Asp3618=
XM_017009966.2:c.10776T>C	XP_016865455.1:p.Asp3592=
XM_017009967.1:c.10761T>C	XP_016865456.1:p.Asp3587=
XM_017009968.2:c.10857T>C	XP_016865457.1:p.Asp3619=
XM_017009969.2:c.10857T>C	XP_016865458.1:p.Asp3619=
XM_017009970.2:c.10857T>C	XP_016865459.1:p.Asp3619=
XM_017009971.2:c.10857T>C	XP_016865460.1:p.Asp3619=
XM_017009972.1:c.3975T>C	XP_016865461.1:p.Asp1325=
XM_017009973.1:c.3954T>C	XP_016865462.1:p.Asp1318=
XM_017009974.2:c.*58T>C	XP_016865463.1:n.*58T>C
NR_003149.2:n.10852T>C