Canonical Allele Identifier: CA766641765

Gene: MLPH

Linked Data

• dbSNP Id: rs1375497897
• MyVariant Identifiers: chr2:g.238462793C>A (hg19) ; chr2:g.237554150C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237554150C>A , CM000664.2:g.237554150C>A	GRCh38
NC_000002.11:g.238462793C>A , CM000664.1:g.238462793C>A	GRCh37
NC_000002.10:g.238127532C>A	NCBI36
NG_007286.1:g.71864C>A , LRG_83:g.71864C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264605.8:c.*558C>A MANE Select	ENSP00000264605.3:n.*558C>A
ENST00000264605.7:c.*558C>A	ENSP00000264605.3:n.*558C>A
NM_001042467.2:c.*558C>A	NP_001035932.1:n.*558C>A
NM_001281473.1:c.*558C>A	NP_001268402.1:n.*558C>A
NM_001281474.1:c.*558C>A	NP_001268403.1:n.*558C>A
NM_024101.6:c.*558C>A	NP_077006.1:n.*558C>A
NR_104019.1:n.2793C>A
NM_024101.7:c.*558C>A MANE Select	NP_077006.1:n.*558C>A
NM_001042467.3:c.*558C>A	NP_001035932.1:n.*558C>A
NM_001281473.2:c.*558C>A	NP_001268402.1:n.*558C>A
NM_001281474.2:c.*558C>A	NP_001268403.1:n.*558C>A
NR_104019.2:n.2761C>A