Canonical Allele Identifier: CA360409529

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041566C>T (hg19) ; chr5:g.90745749C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745749C>T , CM000667.2:g.90745749C>T	GRCh38
NC_000005.9:g.90041566C>T , CM000667.1:g.90041566C>T	GRCh37
NC_000005.8:g.90077322C>T	NCBI36
NG_007083.1:g.191950C>T
NG_007083.2:g.221406C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10928C>T MANE Select	ENSP00000384582.2:p.Thr3643Ile
ENST00000425867.3:c.59C>T	ENSP00000392618.3:p.Thr20Ile
ENST00000639431.1:c.265+69540C>T	ENSP00000491057.1:n.265+69540C>T
ENST00000640374.1:n.4072C>T
ENST00000640464.1:n.1347C>T
ENST00000405460.6:c.10928C>T	ENSP00000384582.2:p.Thr3643Ile
ENST00000509621.1:c.3625C>T
NM_032119.3:c.10928C>T	NP_115495.3:p.Thr3643Ile
NR_003149.1:n.10941C>T
XM_011543675.1:c.10925C>T	XP_011541977.1:p.Thr3642Ile
XM_011543676.1:c.10847C>T	XP_011541978.1:p.Thr3616Ile
XM_011543677.1:c.8231C>T	XP_011541979.1:p.Thr2744Ile
XM_011543678.1:c.10928C>T	XP_011541980.1:p.Thr3643Ile
NM_032119.4:c.10928C>T MANE Select	NP_115495.3:p.Thr3643Ile
XM_017009963.2:c.10949C>T	XP_016865452.1:p.Thr3650Ile
XM_017009964.2:c.10946C>T	XP_016865453.1:p.Thr3649Ile
XM_017009965.1:c.10946C>T	XP_016865454.1:p.Thr3649Ile
XM_017009966.2:c.10868C>T	XP_016865455.1:p.Thr3623Ile
XM_017009967.1:c.10853C>T	XP_016865456.1:p.Thr3618Ile
XM_017009968.2:c.10949C>T	XP_016865457.1:p.Thr3650Ile
XM_017009969.2:c.10949C>T	XP_016865458.1:p.Thr3650Ile
XM_017009970.2:c.10949C>T	XP_016865459.1:p.Thr3650Ile
XM_017009971.2:c.10949C>T	XP_016865460.1:p.Thr3650Ile
XM_017009972.1:c.4067C>T	XP_016865461.1:p.Thr1356Ile
XM_017009973.1:c.4046C>T	XP_016865462.1:p.Thr1349Ile
NR_003149.2:n.10944C>T