Canonical Allele Identifier: CA431686703

Gene: MLPH

Linked Data

• MyVariant Identifiers: chr2:g.238436027T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237527384T>C , CM000664.2:g.237527384T>C	GRCh38
NC_000002.11:g.238436027T>C , CM000664.1:g.238436027T>C	GRCh37
NC_000002.10:g.238100766T>C	NCBI36
NG_007286.1:g.45098T>C , LRG_83:g.45098T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264605.8:c.888T>C MANE Select	ENSP00000264605.3:p.Asn296=
ENST00000264605.7:c.888T>C	ENSP00000264605.3:p.Asn296=
ENST00000338530.8:c.888T>C	ENSP00000341845.4:p.Asn296=
ENST00000409373.5:c.768T>C	ENSP00000386780.1:p.Asn256=
ENST00000410032.5:c.675+7355T>C	ENSP00000386338.1:n.675+7355T>C
ENST00000436965.5:c.134T>C
ENST00000437893.5:c.300+1579T>C	ENSP00000412438.1:n.300+1579T>C
ENST00000464123.5:n.953T>C
ENST00000468178.5:n.1099T>C
ENST00000478712.5:n.567T>C
ENST00000482528.1:n.140T>C
ENST00000485956.1:n.264T>C
ENST00000494110.5:n.568T>C
ENST00000495439.5:n.1265T>C
NM_001042467.2:c.888T>C	NP_001035932.1:p.Asn296=
NM_001281473.1:c.768T>C	NP_001268402.1:p.Asn256=
NM_001281474.1:c.675+7355T>C	NP_001268403.1:n.675+7355T>C
NM_024101.6:c.888T>C	NP_077006.1:p.Asn296=
NR_104019.1:n.1131T>C
XM_006712737.1:c.768T>C	XP_006712800.1:p.Asn256=
XM_006712739.1:c.888T>C	XP_006712802.1:p.Asn296=
XM_006712740.1:c.768T>C	XP_006712803.1:p.Asn256=
XM_011511811.1:c.888T>C	XP_011510113.1:p.Asn296=
XM_011511812.1:c.453T>C	XP_011510114.1:p.Asn151=
XR_923025.1:n.1099T>C
XM_017004893.1:c.888T>C	XP_016860382.1:p.Asn296=
XM_017004894.2:c.888T>C	XP_016860383.1:p.Asn296=
NM_024101.7:c.888T>C MANE Select	NP_077006.1:p.Asn296=
NM_001042467.3:c.888T>C	NP_001035932.1:p.Asn296=
NM_001281473.2:c.768T>C	NP_001268402.1:p.Asn256=
NM_001281474.2:c.675+7355T>C	NP_001268403.1:n.675+7355T>C
NR_104019.2:n.1099T>C