Canonical Allele Identifier: CA360409208

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041510A>T (hg19) ; chr5:g.90745693A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745693A>T , CM000667.2:g.90745693A>T	GRCh38
NC_000005.9:g.90041510A>T , CM000667.1:g.90041510A>T	GRCh37
NC_000005.8:g.90077266A>T	NCBI36
NG_007083.1:g.191894A>T
NG_007083.2:g.221350A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10872A>T MANE Select	ENSP00000384582.2:p.Gln3624His
ENST00000425867.3:c.3A>T	ENSP00000392618.3:p.Gln1His
ENST00000639431.1:c.265+69484A>T	ENSP00000491057.1:n.265+69484A>T
ENST00000640374.1:n.4016A>T
ENST00000640464.1:n.1291A>T
ENST00000405460.6:c.10872A>T	ENSP00000384582.2:p.Gln3624His
ENST00000509621.1:c.3569A>T
NM_032119.3:c.10872A>T	NP_115495.3:p.Gln3624His
NR_003149.1:n.10885A>T
XM_011543675.1:c.10869A>T	XP_011541977.1:p.Gln3623His
XM_011543676.1:c.10791A>T	XP_011541978.1:p.Gln3597His
XM_011543677.1:c.8175A>T	XP_011541979.1:p.Gln2725His
XM_011543678.1:c.10872A>T	XP_011541980.1:p.Gln3624His
NM_032119.4:c.10872A>T MANE Select	NP_115495.3:p.Gln3624His
XM_017009963.2:c.10893A>T	XP_016865452.1:p.Gln3631His
XM_017009964.2:c.10890A>T	XP_016865453.1:p.Gln3630His
XM_017009965.1:c.10890A>T	XP_016865454.1:p.Gln3630His
XM_017009966.2:c.10812A>T	XP_016865455.1:p.Gln3604His
XM_017009967.1:c.10797A>T	XP_016865456.1:p.Gln3599His
XM_017009968.2:c.10893A>T	XP_016865457.1:p.Gln3631His
XM_017009969.2:c.10893A>T	XP_016865458.1:p.Gln3631His
XM_017009970.2:c.10893A>T	XP_016865459.1:p.Gln3631His
XM_017009971.2:c.10893A>T	XP_016865460.1:p.Gln3631His
XM_017009972.1:c.4011A>T	XP_016865461.1:p.Gln1337His
XM_017009973.1:c.3990A>T	XP_016865462.1:p.Gln1330His
NR_003149.2:n.10888A>T