Canonical Allele Identifier: CA2322323129

Gene: S1PR2 DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10223925T= , CM000681.2:g.10223925T=	GRCh38
NC_000019.9:g.10334601T= , CM000681.1:g.10334601T=	GRCh37
NC_000019.8:g.10195601T=	NCBI36
NG_028016.3:g.12362A= , LRG_362:g.12362A=
NG_046802.1:g.12883A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646641.1:c.981A= (S1PR2) MANE Select	ENSP00000496438.1:p.Pro327=
ENST00000588952.5:c.-401-5056A= (DNMT1)	ENSP00000467050.1:n.-401-5056A=
ENST00000590320.2:c.981A= (S1PR2)	ENSP00000466933.1:p.Pro327=
ENST00000592342.5:c.-284+7279A= (DNMT1)	ENSP00000465993.1:n.-284+7279A=
NM_004230.3:c.981A= (S1PR2)	NP_004221.3:p.Pro327=
XM_011528425.1:c.894+87A= (S1PR2)	XP_011526727.1:n.894+87A=
NM_004230.4:c.981A= (S1PR2) MANE Select	NP_004221.3:p.Pro327=