Canonical Allele Identifier: CA15970542
Gene: CSE1L HGNC NCBI

Linked Data

dbSNP Id: rs2075677

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.49084487A>G , CM000682.2:g.49084487A>G GRCh38
NC_000020.10:g.47701024A>G , CM000682.1:g.47701024A>G GRCh37
NC_000020.9:g.47134431A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262982.3:c.1619+325A>G MANE Select ENSP00000262982.2:n.1619+325A>G
ENST00000262982.2:c.1619+325A>G ENSP00000262982.2:n.1619+325A>G
ENST00000396192.7:c.1451+325A>G ENSP00000379495.3:n.1451+325A>G
NM_001256135.1:c.1451+325A>G NP_001243064.1:n.1451+325A>G
NM_001316.3:c.1619+325A>G NP_001307.2:n.1619+325A>G
NR_045796.1:n.1323+325A>G
XM_011528599.1:c.1619+325A>G XP_011526901.1:n.1619+325A>G
NM_001362762.1:c.1619+325A>G NP_001349691.1:n.1619+325A>G
NM_001316.4:c.1619+325A>G MANE Select NP_001307.2:n.1619+325A>G
NM_001362762.2:c.1619+325A>G NP_001349691.1:n.1619+325A>G
NM_001256135.2:c.1451+325A>G NP_001243064.1:n.1451+325A>G
NR_045796.2:n.1257+325A>G