Canonical Allele Identifier: CA360425723

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119383C>G (hg19) ; chr5:g.90823566C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823566C>G , CM000667.2:g.90823566C>G	GRCh38
NC_000005.9:g.90119383C>G , CM000667.1:g.90119383C>G	GRCh37
NC_000005.8:g.90155139C>G	NCBI36
NG_007083.1:g.269767C>G
NG_007083.2:g.299223C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16338C>G MANE Select	ENSP00000384582.2:p.Cys5446Trp
ENST00000425867.3:c.5292C>G	ENSP00000392618.3:p.Cys1764Trp
ENST00000638510.1:n.3605C>G
ENST00000639431.1:c.265+147357C>G	ENSP00000491057.1:n.265+147357C>G
ENST00000640061.1:n.128+1384C>G
ENST00000640407.1:c.2748C>G	ENSP00000491425.1:p.Cys916Trp
ENST00000405460.6:c.16338C>G	ENSP00000384582.2:p.Cys5446Trp
ENST00000425867.2:c.3321C>G	ENSP00000392618.2:p.Cys1107Trp
NM_032119.3:c.16338C>G	NP_115495.3:p.Cys5446Trp
NR_003149.1:n.16351C>G
XM_011543675.1:c.16335C>G	XP_011541977.1:p.Cys5445Trp
XM_011543676.1:c.16257C>G	XP_011541978.1:p.Cys5419Trp
XM_011543677.1:c.13641C>G	XP_011541979.1:p.Cys4547Trp
NM_032119.4:c.16338C>G MANE Select	NP_115495.3:p.Cys5446Trp
XM_017009963.2:c.16359C>G	XP_016865452.1:p.Cys5453Trp
XM_017009964.2:c.16356C>G	XP_016865453.1:p.Cys5452Trp
XM_017009965.1:c.16356C>G	XP_016865454.1:p.Cys5452Trp
XM_017009966.2:c.16278C>G	XP_016865455.1:p.Cys5426Trp
XM_017009967.1:c.16263C>G	XP_016865456.1:p.Cys5421Trp
XM_017009968.2:c.16179C>G	XP_016865457.1:p.Cys5393Trp
XM_017009969.2:c.16359C>G	XP_016865458.1:p.Cys5453Trp
XM_017009972.1:c.9477C>G	XP_016865461.1:p.Cys3159Trp
XM_017009973.1:c.9456C>G	XP_016865462.1:p.Cys3152Trp
NR_003149.2:n.16354C>G