Canonical Allele Identifier: CA351200379

Gene: MLPH

Linked Data

• MyVariant Identifiers: chr2:g.238436038A>T (hg19) ; chr2:g.237527395A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237527395A>T , CM000664.2:g.237527395A>T	GRCh38
NC_000002.11:g.238436038A>T , CM000664.1:g.238436038A>T	GRCh37
NC_000002.10:g.238100777A>T	NCBI36
NG_007286.1:g.45109A>T , LRG_83:g.45109A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264605.8:c.899A>T MANE Select	ENSP00000264605.3:p.Asn300Ile
ENST00000264605.7:c.899A>T	ENSP00000264605.3:p.Asn300Ile
ENST00000338530.8:c.899A>T	ENSP00000341845.4:p.Asn300Ile
ENST00000409373.5:c.779A>T	ENSP00000386780.1:p.Asn260Ile
ENST00000410032.5:c.675+7366A>T	ENSP00000386338.1:n.675+7366A>T
ENST00000436965.5:c.145A>T
ENST00000437893.5:c.300+1590A>T	ENSP00000412438.1:n.300+1590A>T
ENST00000464123.5:n.964A>T
ENST00000468178.5:n.1110A>T
ENST00000478712.5:n.578A>T
ENST00000482528.1:n.151A>T
ENST00000485956.1:n.275A>T
ENST00000494110.5:n.579A>T
ENST00000495439.5:n.1276A>T
NM_001042467.2:c.899A>T	NP_001035932.1:p.Asn300Ile
NM_001281473.1:c.779A>T	NP_001268402.1:p.Asn260Ile
NM_001281474.1:c.675+7366A>T	NP_001268403.1:n.675+7366A>T
NM_024101.6:c.899A>T	NP_077006.1:p.Asn300Ile
NR_104019.1:n.1142A>T
XM_006712737.1:c.779A>T	XP_006712800.1:p.Asn260Ile
XM_006712739.1:c.899A>T	XP_006712802.1:p.Asn300Ile
XM_006712740.1:c.779A>T	XP_006712803.1:p.Asn260Ile
XM_011511811.1:c.899A>T	XP_011510113.1:p.Asn300Ile
XM_011511812.1:c.464A>T	XP_011510114.1:p.Asn155Ile
XR_923025.1:n.1110A>T
XM_017004893.1:c.899A>T	XP_016860382.1:p.Asn300Ile
XM_017004894.2:c.899A>T	XP_016860383.1:p.Asn300Ile
NM_024101.7:c.899A>T MANE Select	NP_077006.1:p.Asn300Ile
NM_001042467.3:c.899A>T	NP_001035932.1:p.Asn300Ile
NM_001281473.2:c.779A>T	NP_001268402.1:p.Asn260Ile
NM_001281474.2:c.675+7366A>T	NP_001268403.1:n.675+7366A>T
NR_104019.2:n.1110A>T