Canonical Allele Identifier: CA766641768

Gene: MLPH

Linked Data

• dbSNP Id: rs1415911272
• gnomAD v3: 2-237554156-C-T
• gnomAD v4: 2-237554156-C-T
• MyVariant Identifiers: chr2:g.238462799C>T (hg19) ; chr2:g.237554156C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237554156C>T , CM000664.2:g.237554156C>T	GRCh38
NC_000002.11:g.238462799C>T , CM000664.1:g.238462799C>T	GRCh37
NC_000002.10:g.238127538C>T	NCBI36
NG_007286.1:g.71870C>T , LRG_83:g.71870C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264605.8:c.*564C>T MANE Select	ENSP00000264605.3:n.*564C>T
ENST00000264605.7:c.*564C>T	ENSP00000264605.3:n.*564C>T
NM_001042467.2:c.*564C>T	NP_001035932.1:n.*564C>T
NM_001281473.1:c.*564C>T	NP_001268402.1:n.*564C>T
NM_001281474.1:c.*564C>T	NP_001268403.1:n.*564C>T
NM_024101.6:c.*564C>T	NP_077006.1:n.*564C>T
NR_104019.1:n.2799C>T
NM_024101.7:c.*564C>T MANE Select	NP_077006.1:n.*564C>T
NM_001042467.3:c.*564C>T	NP_001035932.1:n.*564C>T
NM_001281473.2:c.*564C>T	NP_001268402.1:n.*564C>T
NM_001281474.2:c.*564C>T	NP_001268403.1:n.*564C>T
NR_104019.2:n.2767C>T