Canonical Allele Identifier: CA360401727

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90087032G>T (hg19) ; chr5:g.90791215G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791215G>T , CM000667.2:g.90791215G>T	GRCh38
NC_000005.9:g.90087032G>T , CM000667.1:g.90087032G>T	GRCh37
NC_000005.8:g.90122788G>T	NCBI36
NG_007083.1:g.237416G>T
NG_007083.2:g.266872G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14386G>T MANE Select	ENSP00000384582.2:p.Asp4796Tyr
ENST00000425867.3:c.3340G>T	ENSP00000392618.3:p.Asp1114Tyr
ENST00000507314.2:c.61G>T	ENSP00000491299.1:p.Asp21Tyr
ENST00000638510.1:n.1653G>T
ENST00000638585.1:n.152G>T
ENST00000638975.1:c.1015G>T	ENSP00000492630.1:p.Asp339Tyr
ENST00000639431.1:c.265+115006G>T	ENSP00000491057.1:n.265+115006G>T
ENST00000640407.1:c.796G>T	ENSP00000491425.1:p.Asp266Tyr
ENST00000405460.6:c.14386G>T	ENSP00000384582.2:p.Asp4796Tyr
ENST00000425867.2:c.1369G>T	ENSP00000392618.2:p.Asp457Tyr
ENST00000507314.1:n.61G>T
NM_032119.3:c.14386G>T	NP_115495.3:p.Asp4796Tyr
NR_003149.1:n.14399G>T
XM_011543675.1:c.14383G>T	XP_011541977.1:p.Asp4795Tyr
XM_011543676.1:c.14305G>T	XP_011541978.1:p.Asp4769Tyr
XM_011543677.1:c.11689G>T	XP_011541979.1:p.Asp3897Tyr
XM_011543678.1:c.14386G>T	XP_011541980.1:p.Asp4796Tyr
NM_032119.4:c.14386G>T MANE Select	NP_115495.3:p.Asp4796Tyr
XM_017009963.2:c.14407G>T	XP_016865452.1:p.Asp4803Tyr
XM_017009964.2:c.14404G>T	XP_016865453.1:p.Asp4802Tyr
XM_017009965.1:c.14404G>T	XP_016865454.1:p.Asp4802Tyr
XM_017009966.2:c.14326G>T	XP_016865455.1:p.Asp4776Tyr
XM_017009967.1:c.14311G>T	XP_016865456.1:p.Asp4771Tyr
XM_017009968.2:c.14407G>T	XP_016865457.1:p.Asp4803Tyr
XM_017009969.2:c.14407G>T	XP_016865458.1:p.Asp4803Tyr
XM_017009970.2:c.14407G>T	XP_016865459.1:p.Asp4803Tyr
XM_017009971.2:c.14407G>T	XP_016865460.1:p.Asp4803Tyr
XM_017009972.1:c.7525G>T	XP_016865461.1:p.Asp2509Tyr
XM_017009973.1:c.7504G>T	XP_016865462.1:p.Asp2502Tyr
NR_003149.2:n.14402G>T