Canonical Allele Identifier: CA445436580

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119341T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823524T>A , CM000667.2:g.90823524T>A	GRCh38
NC_000005.9:g.90119341T>A , CM000667.1:g.90119341T>A	GRCh37
NC_000005.8:g.90155097T>A	NCBI36
NG_007083.1:g.269725T>A
NG_007083.2:g.299181T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16296T>A MANE Select	ENSP00000384582.2:p.Ser5432=
ENST00000425867.3:c.5250T>A	ENSP00000392618.3:p.Ser1750=
ENST00000638510.1:n.3563T>A
ENST00000639431.1:c.265+147315T>A	ENSP00000491057.1:n.265+147315T>A
ENST00000640061.1:n.128+1342T>A
ENST00000640407.1:c.2706T>A	ENSP00000491425.1:p.Ser902=
ENST00000405460.6:c.16296T>A	ENSP00000384582.2:p.Ser5432=
ENST00000425867.2:c.3279T>A	ENSP00000392618.2:p.Ser1093=
NM_032119.3:c.16296T>A	NP_115495.3:p.Ser5432=
NR_003149.1:n.16309T>A
XM_011543675.1:c.16293T>A	XP_011541977.1:p.Ser5431=
XM_011543676.1:c.16215T>A	XP_011541978.1:p.Ser5405=
XM_011543677.1:c.13599T>A	XP_011541979.1:p.Ser4533=
NM_032119.4:c.16296T>A MANE Select	NP_115495.3:p.Ser5432=
XM_017009963.2:c.16317T>A	XP_016865452.1:p.Ser5439=
XM_017009964.2:c.16314T>A	XP_016865453.1:p.Ser5438=
XM_017009965.1:c.16314T>A	XP_016865454.1:p.Ser5438=
XM_017009966.2:c.16236T>A	XP_016865455.1:p.Ser5412=
XM_017009967.1:c.16221T>A	XP_016865456.1:p.Ser5407=
XM_017009968.2:c.16137T>A	XP_016865457.1:p.Ser5379=
XM_017009969.2:c.16317T>A	XP_016865458.1:p.Ser5439=
XM_017009972.1:c.9435T>A	XP_016865461.1:p.Ser3145=
XM_017009973.1:c.9414T>A	XP_016865462.1:p.Ser3138=
NR_003149.2:n.16312T>A