Canonical Allele Identifier: CA351200329

Gene: MLPH

Linked Data

• MyVariant Identifiers: chr2:g.238436029T>A (hg19) ; chr2:g.237527386T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237527386T>A , CM000664.2:g.237527386T>A	GRCh38
NC_000002.11:g.238436029T>A , CM000664.1:g.238436029T>A	GRCh37
NC_000002.10:g.238100768T>A	NCBI36
NG_007286.1:g.45100T>A , LRG_83:g.45100T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264605.8:c.890T>A MANE Select	ENSP00000264605.3:p.Val297Asp
ENST00000264605.7:c.890T>A	ENSP00000264605.3:p.Val297Asp
ENST00000338530.8:c.890T>A	ENSP00000341845.4:p.Val297Asp
ENST00000409373.5:c.770T>A	ENSP00000386780.1:p.Val257Asp
ENST00000410032.5:c.675+7357T>A	ENSP00000386338.1:n.675+7357T>A
ENST00000436965.5:c.136T>A
ENST00000437893.5:c.300+1581T>A	ENSP00000412438.1:n.300+1581T>A
ENST00000464123.5:n.955T>A
ENST00000468178.5:n.1101T>A
ENST00000478712.5:n.569T>A
ENST00000482528.1:n.142T>A
ENST00000485956.1:n.266T>A
ENST00000494110.5:n.570T>A
ENST00000495439.5:n.1267T>A
NM_001042467.2:c.890T>A	NP_001035932.1:p.Val297Asp
NM_001281473.1:c.770T>A	NP_001268402.1:p.Val257Asp
NM_001281474.1:c.675+7357T>A	NP_001268403.1:n.675+7357T>A
NM_024101.6:c.890T>A	NP_077006.1:p.Val297Asp
NR_104019.1:n.1133T>A
XM_006712737.1:c.770T>A	XP_006712800.1:p.Val257Asp
XM_006712739.1:c.890T>A	XP_006712802.1:p.Val297Asp
XM_006712740.1:c.770T>A	XP_006712803.1:p.Val257Asp
XM_011511811.1:c.890T>A	XP_011510113.1:p.Val297Asp
XM_011511812.1:c.455T>A	XP_011510114.1:p.Val152Asp
XR_923025.1:n.1101T>A
XM_017004893.1:c.890T>A	XP_016860382.1:p.Val297Asp
XM_017004894.2:c.890T>A	XP_016860383.1:p.Val297Asp
NM_024101.7:c.890T>A MANE Select	NP_077006.1:p.Val297Asp
NM_001042467.3:c.890T>A	NP_001035932.1:p.Val297Asp
NM_001281473.2:c.770T>A	NP_001268402.1:p.Val257Asp
NM_001281474.2:c.675+7357T>A	NP_001268403.1:n.675+7357T>A
NR_104019.2:n.1101T>A