Canonical Allele Identifier: CA2190419

Gene: MLPH

Linked Data

• dbSNP Id: rs374857388
• ExAC: 2:238436106 G / A
• gnomAD v2: 2-238436106-G-A
• gnomAD v3: 2-237527463-G-A
• gnomAD v4: 2-237527463-G-A
• MyVariant Identifiers: chr2:g.238436106G>A (hg19) ; chr2:g.237527463G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237527463G>A , CM000664.2:g.237527463G>A	GRCh38
NC_000002.11:g.238436106G>A , CM000664.1:g.238436106G>A	GRCh37
NC_000002.10:g.238100845G>A	NCBI36
NG_007286.1:g.45177G>A , LRG_83:g.45177G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264605.8:c.967G>A MANE Select	ENSP00000264605.3:p.Val323Met
ENST00000264605.7:c.967G>A	ENSP00000264605.3:p.Val323Met
ENST00000338530.8:c.967G>A	ENSP00000341845.4:p.Val323Met
ENST00000409373.5:c.847G>A	ENSP00000386780.1:p.Val283Met
ENST00000410032.5:c.675+7434G>A	ENSP00000386338.1:n.675+7434G>A
ENST00000415753.5:c.29G>A
ENST00000436965.5:c.213G>A
ENST00000437893.5:c.300+1658G>A	ENSP00000412438.1:n.300+1658G>A
ENST00000464123.5:n.1032G>A
ENST00000468178.5:n.1178G>A
ENST00000478712.5:n.646G>A
ENST00000482528.1:n.219G>A
ENST00000485956.1:n.343G>A
ENST00000494110.5:n.647G>A
ENST00000495439.5:n.1344G>A
NM_001042467.2:c.967G>A	NP_001035932.1:p.Val323Met
NM_001281473.1:c.847G>A	NP_001268402.1:p.Val283Met
NM_001281474.1:c.675+7434G>A	NP_001268403.1:n.675+7434G>A
NM_024101.6:c.967G>A	NP_077006.1:p.Val323Met
NR_104019.1:n.1210G>A
XM_006712737.1:c.847G>A	XP_006712800.1:p.Val283Met
XM_006712739.1:c.967G>A	XP_006712802.1:p.Val323Met
XM_006712740.1:c.847G>A	XP_006712803.1:p.Val283Met
XM_011511811.1:c.967G>A	XP_011510113.1:p.Val323Met
XM_011511812.1:c.532G>A	XP_011510114.1:p.Val178Met
XR_923025.1:n.1178G>A
XM_017004893.1:c.967G>A	XP_016860382.1:p.Val323Met
XM_017004894.2:c.967G>A	XP_016860383.1:p.Val323Met
NM_024101.7:c.967G>A MANE Select	NP_077006.1:p.Val323Met
NM_001042467.3:c.967G>A	NP_001035932.1:p.Val323Met
NM_001281473.2:c.847G>A	NP_001268402.1:p.Val283Met
NM_001281474.2:c.675+7434G>A	NP_001268403.1:n.675+7434G>A
NR_104019.2:n.1178G>A