Canonical Allele Identifier: CA920056721

Gene: S1PR2 DNMT1

Linked Data

• dbSNP Id: rs1568275383

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10224503_10224504insTGCAGGTGTGGAGCTGAGAATAGCTTGGGGGGTGGCTGTTTTTG , CM000681.2:g.10224503_10224504insTGCAGGTGTGGAGCTGAGAATAGCTTGGGGGGTGGCTGTTTTTG	GRCh38
NC_000019.9:g.10335179_10335180insTGCAGGTGTGGAGCTGAGAATAGCTTGGGGGGTGGCTGTTTTTG , CM000681.1:g.10335179_10335180insTGCAGGTGTGGAGCTGAGAATAGCTTGGGGGGTGGCTGTTTTTG	GRCh37
NC_000019.8:g.10196179_10196180insTGCAGGTGTGGAGCTGAGAATAGCTTGGGGGGTGGCTGTTTTTG	NCBI36
NG_028016.3:g.11783_11784insCAAAAACAGCCACCCCCCAAGCTATTCTCAGCTCCACACCTGCA , LRG_362:g.11783_11784insCAAAAACAGCCACCCCCCAAGCTATTCTCAGCTCCACACCTGCA
NG_046802.1:g.12304_12305insCAAAAACAGCCACCCCCCAAGCTATTCTCAGCTCCACACCTGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646641.1:c.402_403insCAAAAACAGCCACCCCCCAAGCTATTCTCAGCTCCACACCTGCA (S1PR2) MANE Select	ENSP00000496438.1:p.Ala135GlnfsTer?
ENST00000588952.5:c.-401-5635_-401-5634insCAAAAACAGCCACCCCCCAAGCTATTCTCAGCTCCACACCTGCA (DNMT1)	ENSP00000467050.1:n.-401-5635_-401-5634insCAAAAACAGCCACCCCCCA...
ENST00000590320.2:c.402_403insCAAAAACAGCCACCCCCCAAGCTATTCTCAGCTCCACACCTGCA (S1PR2)	ENSP00000466933.1:p.Ala135GlnfsTer?
ENST00000592342.5:c.-284+6700_-284+6701insCAAAAACAGCCACCCCCCAAGCTATTCTCAGCTCCACACCTGCA (DNMT1)	ENSP00000465993.1:n.-284+6700_-284+6701insCAAAAACAGCCACCCCCCA...
NM_004230.3:c.402_403insCAAAAACAGCCACCCCCCAAGCTATTCTCAGCTCCACACCTGCA (S1PR2)	NP_004221.3:p.Ala135GlnfsTer?
XM_011528425.1:c.402_403insCAAAAACAGCCACCCCCCAAGCTATTCTCAGCTCCACACCTGCA (S1PR2)	XP_011526727.1:p.Ala135GlnfsTer?
NM_004230.4:c.402_403insCAAAAACAGCCACCCCCCAAGCTATTCTCAGCTCCACACCTGCA (S1PR2) MANE Select	NP_004221.3:p.Ala135GlnfsTer?