Canonical Allele Identifier: CA351200343

Gene: MLPH

Linked Data

• MyVariant Identifiers: chr2:g.238436032T>A (hg19) ; chr2:g.237527389T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237527389T>A , CM000664.2:g.237527389T>A	GRCh38
NC_000002.11:g.238436032T>A , CM000664.1:g.238436032T>A	GRCh37
NC_000002.10:g.238100771T>A	NCBI36
NG_007286.1:g.45103T>A , LRG_83:g.45103T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264605.8:c.893T>A MANE Select	ENSP00000264605.3:p.Ile298Asn
ENST00000264605.7:c.893T>A	ENSP00000264605.3:p.Ile298Asn
ENST00000338530.8:c.893T>A	ENSP00000341845.4:p.Ile298Asn
ENST00000409373.5:c.773T>A	ENSP00000386780.1:p.Ile258Asn
ENST00000410032.5:c.675+7360T>A	ENSP00000386338.1:n.675+7360T>A
ENST00000436965.5:c.139T>A
ENST00000437893.5:c.300+1584T>A	ENSP00000412438.1:n.300+1584T>A
ENST00000464123.5:n.958T>A
ENST00000468178.5:n.1104T>A
ENST00000478712.5:n.572T>A
ENST00000482528.1:n.145T>A
ENST00000485956.1:n.269T>A
ENST00000494110.5:n.573T>A
ENST00000495439.5:n.1270T>A
NM_001042467.2:c.893T>A	NP_001035932.1:p.Ile298Asn
NM_001281473.1:c.773T>A	NP_001268402.1:p.Ile258Asn
NM_001281474.1:c.675+7360T>A	NP_001268403.1:n.675+7360T>A
NM_024101.6:c.893T>A	NP_077006.1:p.Ile298Asn
NR_104019.1:n.1136T>A
XM_006712737.1:c.773T>A	XP_006712800.1:p.Ile258Asn
XM_006712739.1:c.893T>A	XP_006712802.1:p.Ile298Asn
XM_006712740.1:c.773T>A	XP_006712803.1:p.Ile258Asn
XM_011511811.1:c.893T>A	XP_011510113.1:p.Ile298Asn
XM_011511812.1:c.458T>A	XP_011510114.1:p.Ile153Asn
XR_923025.1:n.1104T>A
XM_017004893.1:c.893T>A	XP_016860382.1:p.Ile298Asn
XM_017004894.2:c.893T>A	XP_016860383.1:p.Ile298Asn
NM_024101.7:c.893T>A MANE Select	NP_077006.1:p.Ile298Asn
NM_001042467.3:c.893T>A	NP_001035932.1:p.Ile298Asn
NM_001281473.2:c.773T>A	NP_001268402.1:p.Ile258Asn
NM_001281474.2:c.675+7360T>A	NP_001268403.1:n.675+7360T>A
NR_104019.2:n.1104T>A