Canonical Allele Identifier: CA500068467

Gene: MLX

Linked Data

• MyVariant Identifiers: chr17:g.40723597C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571579C>T , CM000679.2:g.42571579C>T	GRCh38
NC_000017.10:g.40723597C>T , CM000679.1:g.40723597C>T	GRCh37
NC_000017.9:g.37977123C>T	NCBI36
NG_029442.1:g.9520C>T
NG_031960.1:g.11253G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.711C>T MANE Select	ENSP00000416627.1:p.His237=
ENST00000246912.8:c.873C>T	ENSP00000246912.3:p.His291=
ENST00000346833.8:c.621C>T	ENSP00000320913.3:p.His207=
ENST00000435881.6:c.711C>T	ENSP00000416627.1:p.His237=
ENST00000585403.5:n.918C>T
ENST00000588320.1:n.1187C>T
ENST00000590050.5:n.877C>T
NM_170607.2:c.873C>T	NP_733752.1:p.His291=
NM_198204.1:c.711C>T	NP_937847.1:p.His237=
NM_198205.1:c.621C>T	NP_937848.1:p.His207=
NM_198204.2:c.711C>T MANE Select	NP_937847.1:p.His237=
NM_170607.3:c.873C>T	NP_733752.1:p.His291=
NM_198205.2:c.621C>T	NP_937848.1:p.His207=