Canonical Allele Identifier: CA1337695053

Gene: MLPH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237527269_237527270delinsCT , CM000664.2:g.237527269_237527270delinsCT	GRCh38
NC_000002.11:g.238435912_238435913delinsCT , CM000664.1:g.238435912_238435913delinsCT	GRCh37
NC_000002.10:g.238100651_238100652delinsCT	NCBI36
NG_007286.1:g.44983_44984delinsCT , LRG_83:g.44983_44984delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264605.8:c.881-108_881-107delinsCT MANE Select	ENSP00000264605.3:n.881-108_881-107delinsCT
ENST00000264605.7:c.881-108_881-107delinsCT	ENSP00000264605.3:n.881-108_881-107delinsCT
ENST00000338530.8:c.881-108_881-107delinsCT	ENSP00000341845.4:n.881-108_881-107delinsCT
ENST00000409373.5:c.761-108_761-107delinsCT	ENSP00000386780.1:n.761-108_761-107delinsCT
ENST00000410032.5:c.675+7240_675+7241delinsCT	ENSP00000386338.1:n.675+7240_675+7241delinsCT
ENST00000436965.5:c.79-60_79-59delinsCT
ENST00000437893.5:c.300+1464_300+1465delinsCT	ENSP00000412438.1:n.300+1464_300+1465delinsCT
ENST00000464123.5:n.946-108_946-107delinsCT
ENST00000468178.5:n.1092-108_1092-107delinsCT
ENST00000478712.5:n.560-108_560-107delinsCT
ENST00000482528.1:n.133-108_133-107delinsCT
ENST00000485956.1:n.257-108_257-107delinsCT
ENST00000494110.5:n.561-108_561-107delinsCT
ENST00000495439.5:n.1258-108_1258-107delinsCT
NM_001042467.2:c.881-108_881-107delinsCT	NP_001035932.1:n.881-108_881-107delinsCT
NM_001281473.1:c.761-108_761-107delinsCT	NP_001268402.1:n.761-108_761-107delinsCT
NM_001281474.1:c.675+7240_675+7241delinsCT	NP_001268403.1:n.675+7240_675+7241delinsCT
NM_024101.6:c.881-108_881-107delinsCT	NP_077006.1:n.881-108_881-107delinsCT
NR_104019.1:n.1124-108_1124-107delinsCT
XM_006712737.1:c.761-108_761-107delinsCT	XP_006712800.1:n.761-108_761-107delinsCT
XM_006712739.1:c.881-108_881-107delinsCT	XP_006712802.1:n.881-108_881-107delinsCT
XM_006712740.1:c.761-108_761-107delinsCT	XP_006712803.1:n.761-108_761-107delinsCT
XM_011511811.1:c.881-108_881-107delinsCT	XP_011510113.1:n.881-108_881-107delinsCT
XM_011511812.1:c.446-108_446-107delinsCT	XP_011510114.1:n.446-108_446-107delinsCT
XR_923025.1:n.1092-108_1092-107delinsCT
XM_017004893.1:c.881-108_881-107delinsCT	XP_016860382.1:n.881-108_881-107delinsCT
XM_017004894.2:c.881-108_881-107delinsCT	XP_016860383.1:n.881-108_881-107delinsCT
NM_024101.7:c.881-108_881-107delinsCT MANE Select	NP_077006.1:n.881-108_881-107delinsCT
NM_001042467.3:c.881-108_881-107delinsCT	NP_001035932.1:n.881-108_881-107delinsCT
NM_001281473.2:c.761-108_761-107delinsCT	NP_001268402.1:n.761-108_761-107delinsCT
NM_001281474.2:c.675+7240_675+7241delinsCT	NP_001268403.1:n.675+7240_675+7241delinsCT
NR_104019.2:n.1092-108_1092-107delinsCT