Canonical Allele Identifier: CA360425678

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1385208222
• MyVariant Identifiers: chr5:g.90119363A>T (hg19) ; chr5:g.90823546A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823546A>T , CM000667.2:g.90823546A>T	GRCh38
NC_000005.9:g.90119363A>T , CM000667.1:g.90119363A>T	GRCh37
NC_000005.8:g.90155119A>T	NCBI36
NG_007083.1:g.269747A>T
NG_007083.2:g.299203A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16318A>T MANE Select	ENSP00000384582.2:p.Thr5440Ser
ENST00000425867.3:c.5272A>T	ENSP00000392618.3:p.Thr1758Ser
ENST00000638510.1:n.3585A>T
ENST00000639431.1:c.265+147337A>T	ENSP00000491057.1:n.265+147337A>T
ENST00000640061.1:n.128+1364A>T
ENST00000640407.1:c.2728A>T	ENSP00000491425.1:p.Thr910Ser
ENST00000405460.6:c.16318A>T	ENSP00000384582.2:p.Thr5440Ser
ENST00000425867.2:c.3301A>T	ENSP00000392618.2:p.Thr1101Ser
NM_032119.3:c.16318A>T	NP_115495.3:p.Thr5440Ser
NR_003149.1:n.16331A>T
XM_011543675.1:c.16315A>T	XP_011541977.1:p.Thr5439Ser
XM_011543676.1:c.16237A>T	XP_011541978.1:p.Thr5413Ser
XM_011543677.1:c.13621A>T	XP_011541979.1:p.Thr4541Ser
NM_032119.4:c.16318A>T MANE Select	NP_115495.3:p.Thr5440Ser
XM_017009963.2:c.16339A>T	XP_016865452.1:p.Thr5447Ser
XM_017009964.2:c.16336A>T	XP_016865453.1:p.Thr5446Ser
XM_017009965.1:c.16336A>T	XP_016865454.1:p.Thr5446Ser
XM_017009966.2:c.16258A>T	XP_016865455.1:p.Thr5420Ser
XM_017009967.1:c.16243A>T	XP_016865456.1:p.Thr5415Ser
XM_017009968.2:c.16159A>T	XP_016865457.1:p.Thr5387Ser
XM_017009969.2:c.16339A>T	XP_016865458.1:p.Thr5447Ser
XM_017009972.1:c.9457A>T	XP_016865461.1:p.Thr3153Ser
XM_017009973.1:c.9436A>T	XP_016865462.1:p.Thr3146Ser
NR_003149.2:n.16334A>T