Canonical Allele Identifier: CA360390816

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89940597A>T (hg19) ; chr5:g.90644780A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90644780A>T , CM000667.2:g.90644780A>T	GRCh38
NC_000005.9:g.89940597A>T , CM000667.1:g.89940597A>T	GRCh37
NC_000005.8:g.89976353A>T	NCBI36
NG_007083.1:g.90981A>T
NG_007083.2:g.120437A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.2809A>T MANE Select	ENSP00000384582.2:p.Thr937Ser
ENST00000504142.2:n.1575A>T
ENST00000639676.1:n.407A>T
ENST00000640403.1:c.112A>T	ENSP00000492531.1:p.Thr38Ser
ENST00000405460.6:c.2809A>T	ENSP00000384582.2:p.Thr937Ser
ENST00000504142.1:c.1574A>T
NM_032119.3:c.2809A>T	NP_115495.3:p.Thr937Ser
NR_003149.1:n.2905A>T
XM_011543675.1:c.2809A>T	XP_011541977.1:p.Thr937Ser
XM_011543676.1:c.2809A>T	XP_011541978.1:p.Thr937Ser
XM_011543677.1:c.112A>T	XP_011541979.1:p.Thr38Ser
XM_011543678.1:c.2809A>T	XP_011541980.1:p.Thr937Ser
XM_011543679.1:c.2809A>T	XP_011541981.1:p.Thr937Ser
NM_032119.4:c.2809A>T MANE Select	NP_115495.3:p.Thr937Ser
XM_017009963.2:c.2809A>T	XP_016865452.1:p.Thr937Ser
XM_017009964.2:c.2809A>T	XP_016865453.1:p.Thr937Ser
XM_017009965.1:c.2806A>T	XP_016865454.1:p.Thr936Ser
XM_017009966.2:c.2809A>T	XP_016865455.1:p.Thr937Ser
XM_017009967.1:c.2713A>T	XP_016865456.1:p.Thr905Ser
XM_017009968.2:c.2809A>T	XP_016865457.1:p.Thr937Ser
XM_017009969.2:c.2809A>T	XP_016865458.1:p.Thr937Ser
XM_017009970.2:c.2809A>T	XP_016865459.1:p.Thr937Ser
XM_017009971.2:c.2809A>T	XP_016865460.1:p.Thr937Ser
XM_017009974.2:c.2809A>T	XP_016865463.1:p.Thr937Ser
NR_003149.2:n.2908A>T