Canonical Allele Identifier: CA2663808792

Gene: MLPH

Linked Data

• gnomAD v4: 2-237554251-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237554251A>G , CM000664.2:g.237554251A>G	GRCh38
NC_000002.11:g.238462894A>G , CM000664.1:g.238462894A>G	GRCh37
NC_000002.10:g.238127633A>G	NCBI36
NG_007286.1:g.71965A>G , LRG_83:g.71965A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264605.8:c.*659A>G MANE Select	ENSP00000264605.3:n.*659A>G
ENST00000264605.7:c.*659A>G	ENSP00000264605.3:n.*659A>G
NM_001042467.2:c.*659A>G	NP_001035932.1:n.*659A>G
NM_001281473.1:c.*659A>G	NP_001268402.1:n.*659A>G
NM_001281474.1:c.*659A>G	NP_001268403.1:n.*659A>G
NM_024101.6:c.*659A>G	NP_077006.1:n.*659A>G
NR_104019.1:n.2894A>G
NM_024101.7:c.*659A>G MANE Select	NP_077006.1:n.*659A>G
NM_001042467.3:c.*659A>G	NP_001035932.1:n.*659A>G
NM_001281473.2:c.*659A>G	NP_001268402.1:n.*659A>G
NM_001281474.2:c.*659A>G	NP_001268403.1:n.*659A>G
NR_104019.2:n.2862A>G