Canonical Allele Identifier: CA360410722

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106825G>T (hg19) ; chr5:g.90811008G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811008G>T , CM000667.2:g.90811008G>T	GRCh38
NC_000005.9:g.90106825G>T , CM000667.1:g.90106825G>T	GRCh37
NC_000005.8:g.90142581G>T	NCBI36
NG_007083.1:g.257209G>T
NG_007083.2:g.286665G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15748G>T MANE Select	ENSP00000384582.2:p.Gly5250Trp
ENST00000425867.3:c.4702G>T	ENSP00000392618.3:p.Gly1568Trp
ENST00000638510.1:n.3015G>T
ENST00000639431.1:c.265+134799G>T	ENSP00000491057.1:n.265+134799G>T
ENST00000640407.1:c.2158G>T	ENSP00000491425.1:p.Gly720Trp
ENST00000405460.6:c.15748G>T	ENSP00000384582.2:p.Gly5250Trp
ENST00000425867.2:c.2731G>T	ENSP00000392618.2:p.Gly911Trp
NM_032119.3:c.15748G>T	NP_115495.3:p.Gly5250Trp
NR_003149.1:n.15761G>T
XM_011543675.1:c.15745G>T	XP_011541977.1:p.Gly5249Trp
XM_011543676.1:c.15667G>T	XP_011541978.1:p.Gly5223Trp
XM_011543677.1:c.13051G>T	XP_011541979.1:p.Gly4351Trp
NM_032119.4:c.15748G>T MANE Select	NP_115495.3:p.Gly5250Trp
XM_017009963.2:c.15769G>T	XP_016865452.1:p.Gly5257Trp
XM_017009964.2:c.15766G>T	XP_016865453.1:p.Gly5256Trp
XM_017009965.1:c.15766G>T	XP_016865454.1:p.Gly5256Trp
XM_017009966.2:c.15688G>T	XP_016865455.1:p.Gly5230Trp
XM_017009967.1:c.15673G>T	XP_016865456.1:p.Gly5225Trp
XM_017009968.2:c.15589G>T	XP_016865457.1:p.Gly5197Trp
XM_017009969.2:c.15769G>T	XP_016865458.1:p.Gly5257Trp
XM_017009972.1:c.8887G>T	XP_016865461.1:p.Gly2963Trp
XM_017009973.1:c.8866G>T	XP_016865462.1:p.Gly2956Trp
NR_003149.2:n.15764G>T