Canonical Allele Identifier: CA2322323079

Gene: S1PR2 DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10223822_10223825delinsGGTT , CM000681.2:g.10223822_10223825delinsGGTT	GRCh38
NC_000019.9:g.10334498_10334501delinsGGTT , CM000681.1:g.10334498_10334501delinsGGTT	GRCh37
NC_000019.8:g.10195498_10195501delinsGGTT	NCBI36
NG_028016.3:g.12462_12465delinsAACC , LRG_362:g.12462_12465delinsAACC
NG_046802.1:g.12983_12986delinsAACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646641.1:c.*19_*22delinsAACC (S1PR2) MANE Select	ENSP00000496438.1:n.*19_*22delinsAACC
ENST00000588952.5:c.-401-4956_-401-4953delinsAACC (DNMT1)	ENSP00000467050.1:n.-401-4956_-401-4953delinsAACC
ENST00000590320.2:c.*19_*22delinsAACC (S1PR2)	ENSP00000466933.1:n.*19_*22delinsAACC
ENST00000592342.5:c.-284+7379_-284+7382delinsAACC (DNMT1)	ENSP00000465993.1:n.-284+7379_-284+7382delinsAACC
NM_004230.3:c.*19_*22delinsAACC (S1PR2)	NP_004221.3:n.*19_*22delinsAACC
XM_011528425.1:c.894+187_894+190delinsAACC (S1PR2)	XP_011526727.1:n.894+187_894+190delinsAACC
NM_004230.4:c.*19_*22delinsAACC (S1PR2) MANE Select	NP_004221.3:n.*19_*22delinsAACC