Canonical Allele Identifier: CA2322323361

Gene: S1PR2 DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10224415C= , CM000681.2:g.10224415C=	GRCh38
NC_000019.9:g.10335091C= , CM000681.1:g.10335091C=	GRCh37
NC_000019.8:g.10196091C=	NCBI36
NG_028016.3:g.11872G= , LRG_362:g.11872G=
NG_046802.1:g.12393G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000646641.1:c.491G= (S1PR2) MANE Select	ENSP00000496438.1:p.Gly164=
ENST00000588952.5:c.-401-5546G= (DNMT1)	ENSP00000467050.1:n.-401-5546G=
ENST00000590320.2:c.491G= (S1PR2)	ENSP00000466933.1:p.Gly164=
ENST00000592342.5:c.-284+6789G= (DNMT1)	ENSP00000465993.1:n.-284+6789G=
NM_004230.3:c.491G= (S1PR2)	NP_004221.3:p.Gly164=
XM_011528425.1:c.491G= (S1PR2)	XP_011526727.1:p.Gly164=
NM_004230.4:c.491G= (S1PR2) MANE Select	NP_004221.3:p.Gly164=