Canonical Allele Identifier: CA2068716282

Gene: MPHOSPH9

Linked Data

• dbSNP Id: rs1727313

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123156306C>A , CM000674.2:g.123156306C>A	GRCh38
NC_000012.11:g.123640853C>A , CM000674.1:g.123640853C>A	GRCh37
NC_000012.10:g.122206806C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000606320.6:c.*501G>T MANE Select	ENSP00000475489.1:n.*501G>T
ENST00000541076.6:c.*501G>T	ENSP00000445859.2:n.*501G>T
ENST00000541603.6:c.555-3681G>T
ENST00000606320.5:c.*501G>T	ENSP00000475489.1:n.*501G>T
XM_006719188.2:c.*501G>T	XP_006719251.1:n.*501G>T
XM_006719189.2:c.*501G>T	XP_006719252.1:n.*501G>T
XM_006719191.2:c.*501G>T	XP_006719254.1:n.*501G>T
XM_006719192.2:c.*501G>T	XP_006719255.1:n.*501G>T
XM_011537736.1:c.*501G>T	XP_011536038.1:n.*501G>T
XM_011537737.1:c.*501G>T	XP_011536039.1:n.*501G>T
XM_011537738.1:c.*501G>T	XP_011536040.1:n.*501G>T
XM_011537739.1:c.3451-3681G>T	XP_011536041.1:n.3451-3681G>T
XM_011537740.1:c.3451-1876G>T	XP_011536042.1:n.3451-1876G>T
XM_011537741.1:c.3451-1876G>T	XP_011536043.1:n.3451-1876G>T
XM_011537742.1:c.*501G>T	XP_011536044.1:n.*501G>T
XM_011537743.1:c.*501G>T	XP_011536045.1:n.*501G>T
XM_011537744.1:c.*501G>T	XP_011536046.1:n.*501G>T
XM_011537746.1:c.*501G>T	XP_011536048.1:n.*501G>T
XM_011537748.1:c.*904G>T	XP_011536050.1:n.*904G>T
XM_011537740.2:c.3451-1876G>T	XP_011536042.1:n.3451-1876G>T
XM_011537741.2:c.3451-1876G>T	XP_011536043.1:n.3451-1876G>T
XM_017018677.1:c.*501G>T	XP_016874166.1:n.*501G>T
XR_001748539.1:n.4307G>T
XR_001748541.1:n.3651-1876G>T
NM_022782.4:c.*501G>T MANE Select	NP_073619.3:n.*501G>T
NR_103517.2:n.4017G>T