Canonical Allele Identifier: CA360425758

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119398A>T (hg19) ; chr5:g.90823581A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823581A>T , CM000667.2:g.90823581A>T	GRCh38
NC_000005.9:g.90119398A>T , CM000667.1:g.90119398A>T	GRCh37
NC_000005.8:g.90155154A>T	NCBI36
NG_007083.1:g.269782A>T
NG_007083.2:g.299238A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16353A>T MANE Select	ENSP00000384582.2:p.Glu5451Asp
ENST00000425867.3:c.5307A>T	ENSP00000392618.3:p.Glu1769Asp
ENST00000638510.1:n.3620A>T
ENST00000639431.1:c.265+147372A>T	ENSP00000491057.1:n.265+147372A>T
ENST00000640061.1:n.128+1399A>T
ENST00000640407.1:c.2763A>T	ENSP00000491425.1:p.Glu921Asp
ENST00000405460.6:c.16353A>T	ENSP00000384582.2:p.Glu5451Asp
ENST00000425867.2:c.3336A>T	ENSP00000392618.2:p.Glu1112Asp
NM_032119.3:c.16353A>T	NP_115495.3:p.Glu5451Asp
NR_003149.1:n.16366A>T
XM_011543675.1:c.16350A>T	XP_011541977.1:p.Glu5450Asp
XM_011543676.1:c.16272A>T	XP_011541978.1:p.Glu5424Asp
XM_011543677.1:c.13656A>T	XP_011541979.1:p.Glu4552Asp
NM_032119.4:c.16353A>T MANE Select	NP_115495.3:p.Glu5451Asp
XM_017009963.2:c.16374A>T	XP_016865452.1:p.Glu5458Asp
XM_017009964.2:c.16371A>T	XP_016865453.1:p.Glu5457Asp
XM_017009965.1:c.16371A>T	XP_016865454.1:p.Glu5457Asp
XM_017009966.2:c.16293A>T	XP_016865455.1:p.Glu5431Asp
XM_017009967.1:c.16278A>T	XP_016865456.1:p.Glu5426Asp
XM_017009968.2:c.16194A>T	XP_016865457.1:p.Glu5398Asp
XM_017009969.2:c.16374A>T	XP_016865458.1:p.Glu5458Asp
XM_017009972.1:c.9492A>T	XP_016865461.1:p.Glu3164Asp
XM_017009973.1:c.9471A>T	XP_016865462.1:p.Glu3157Asp
NR_003149.2:n.16369A>T