Canonical Allele Identifier: CA360401245

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086919A>T (hg19) ; chr5:g.90791102A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791102A>T , CM000667.2:g.90791102A>T	GRCh38
NC_000005.9:g.90086919A>T , CM000667.1:g.90086919A>T	GRCh37
NC_000005.8:g.90122675A>T	NCBI36
NG_007083.1:g.237303A>T
NG_007083.2:g.266759A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14273A>T MANE Select	ENSP00000384582.2:p.Asp4758Val
ENST00000425867.3:c.3227A>T	ENSP00000392618.3:p.Asp1076Val
ENST00000638510.1:n.1540A>T
ENST00000638585.1:n.39A>T
ENST00000638975.1:c.902A>T	ENSP00000492630.1:p.Asp301Val
ENST00000639431.1:c.265+114893A>T	ENSP00000491057.1:n.265+114893A>T
ENST00000640407.1:c.683A>T	ENSP00000491425.1:p.Asp228Val
ENST00000405460.6:c.14273A>T	ENSP00000384582.2:p.Asp4758Val
ENST00000425867.2:c.1256A>T	ENSP00000392618.2:p.Asp419Val
NM_032119.3:c.14273A>T	NP_115495.3:p.Asp4758Val
NR_003149.1:n.14286A>T
XM_011543675.1:c.14270A>T	XP_011541977.1:p.Asp4757Val
XM_011543676.1:c.14192A>T	XP_011541978.1:p.Asp4731Val
XM_011543677.1:c.11576A>T	XP_011541979.1:p.Asp3859Val
XM_011543678.1:c.14273A>T	XP_011541980.1:p.Asp4758Val
NM_032119.4:c.14273A>T MANE Select	NP_115495.3:p.Asp4758Val
XM_017009963.2:c.14294A>T	XP_016865452.1:p.Asp4765Val
XM_017009964.2:c.14291A>T	XP_016865453.1:p.Asp4764Val
XM_017009965.1:c.14291A>T	XP_016865454.1:p.Asp4764Val
XM_017009966.2:c.14213A>T	XP_016865455.1:p.Asp4738Val
XM_017009967.1:c.14198A>T	XP_016865456.1:p.Asp4733Val
XM_017009968.2:c.14294A>T	XP_016865457.1:p.Asp4765Val
XM_017009969.2:c.14294A>T	XP_016865458.1:p.Asp4765Val
XM_017009970.2:c.14294A>T	XP_016865459.1:p.Asp4765Val
XM_017009971.2:c.14294A>T	XP_016865460.1:p.Asp4765Val
XM_017009972.1:c.7412A>T	XP_016865461.1:p.Asp2471Val
XM_017009973.1:c.7391A>T	XP_016865462.1:p.Asp2464Val
NR_003149.2:n.14289A>T