Canonical Allele Identifier: CA445436603

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119377A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823560A>C , CM000667.2:g.90823560A>C	GRCh38
NC_000005.9:g.90119377A>C , CM000667.1:g.90119377A>C	GRCh37
NC_000005.8:g.90155133A>C	NCBI36
NG_007083.1:g.269761A>C
NG_007083.2:g.299217A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16332A>C MANE Select	ENSP00000384582.2:p.Thr5444=
ENST00000425867.3:c.5286A>C	ENSP00000392618.3:p.Thr1762=
ENST00000638510.1:n.3599A>C
ENST00000639431.1:c.265+147351A>C	ENSP00000491057.1:n.265+147351A>C
ENST00000640061.1:n.128+1378A>C
ENST00000640407.1:c.2742A>C	ENSP00000491425.1:p.Thr914=
ENST00000405460.6:c.16332A>C	ENSP00000384582.2:p.Thr5444=
ENST00000425867.2:c.3315A>C	ENSP00000392618.2:p.Thr1105=
NM_032119.3:c.16332A>C	NP_115495.3:p.Thr5444=
NR_003149.1:n.16345A>C
XM_011543675.1:c.16329A>C	XP_011541977.1:p.Thr5443=
XM_011543676.1:c.16251A>C	XP_011541978.1:p.Thr5417=
XM_011543677.1:c.13635A>C	XP_011541979.1:p.Thr4545=
NM_032119.4:c.16332A>C MANE Select	NP_115495.3:p.Thr5444=
XM_017009963.2:c.16353A>C	XP_016865452.1:p.Thr5451=
XM_017009964.2:c.16350A>C	XP_016865453.1:p.Thr5450=
XM_017009965.1:c.16350A>C	XP_016865454.1:p.Thr5450=
XM_017009966.2:c.16272A>C	XP_016865455.1:p.Thr5424=
XM_017009967.1:c.16257A>C	XP_016865456.1:p.Thr5419=
XM_017009968.2:c.16173A>C	XP_016865457.1:p.Thr5391=
XM_017009969.2:c.16353A>C	XP_016865458.1:p.Thr5451=
XM_017009972.1:c.9471A>C	XP_016865461.1:p.Thr3157=
XM_017009973.1:c.9450A>C	XP_016865462.1:p.Thr3150=
NR_003149.2:n.16348A>C