Canonical Allele Identifier: CA445436489

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119281T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823464T>C , CM000667.2:g.90823464T>C	GRCh38
NC_000005.9:g.90119281T>C , CM000667.1:g.90119281T>C	GRCh37
NC_000005.8:g.90155037T>C	NCBI36
NG_007083.1:g.269665T>C
NG_007083.2:g.299121T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16236T>C MANE Select	ENSP00000384582.2:p.Leu5412=
ENST00000425867.3:c.5190T>C	ENSP00000392618.3:p.Leu1730=
ENST00000638510.1:n.3503T>C
ENST00000639431.1:c.265+147255T>C	ENSP00000491057.1:n.265+147255T>C
ENST00000640061.1:n.128+1282T>C
ENST00000640407.1:c.2646T>C	ENSP00000491425.1:p.Leu882=
ENST00000405460.6:c.16236T>C	ENSP00000384582.2:p.Leu5412=
ENST00000425867.2:c.3219T>C	ENSP00000392618.2:p.Leu1073=
NM_032119.3:c.16236T>C	NP_115495.3:p.Leu5412=
NR_003149.1:n.16249T>C
XM_011543675.1:c.16233T>C	XP_011541977.1:p.Leu5411=
XM_011543676.1:c.16155T>C	XP_011541978.1:p.Leu5385=
XM_011543677.1:c.13539T>C	XP_011541979.1:p.Leu4513=
NM_032119.4:c.16236T>C MANE Select	NP_115495.3:p.Leu5412=
XM_017009963.2:c.16257T>C	XP_016865452.1:p.Leu5419=
XM_017009964.2:c.16254T>C	XP_016865453.1:p.Leu5418=
XM_017009965.1:c.16254T>C	XP_016865454.1:p.Leu5418=
XM_017009966.2:c.16176T>C	XP_016865455.1:p.Leu5392=
XM_017009967.1:c.16161T>C	XP_016865456.1:p.Leu5387=
XM_017009968.2:c.16077T>C	XP_016865457.1:p.Leu5359=
XM_017009969.2:c.16257T>C	XP_016865458.1:p.Leu5419=
XM_017009972.1:c.9375T>C	XP_016865461.1:p.Leu3125=
XM_017009973.1:c.9354T>C	XP_016865462.1:p.Leu3118=
NR_003149.2:n.16252T>C