Canonical Allele Identifier: CA390031414
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076536G>A , CM000676.2:g.65076536G>A GRCh38
NC_000014.8:g.65543254G>A , CM000676.1:g.65543254G>A GRCh37
NC_000014.7:g.64613007G>A NCBI36
NG_029830.1:g.30974C>T , LRG_530:g.30974C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.204C>T ENSP00000452206.2:p.Ser68=
ENST00000556979.6:c.*876C>T ENSP00000452378.1:n.*876C>T
ENST00000358664.9:c.423C>T MANE Select ENSP00000351490.4:p.Ser141=
ENST00000651648.1:c.145-6167C>T ENSP00000498863.1:n.145-6167C>T
ENST00000284165.10:c.*1267C>T ENSP00000284165.6:n.*1267C>T
ENST00000341653.6:c.171+17172C>T ENSP00000342482.2:n.171+17172C>T
ENST00000358402.8:c.396C>T ENSP00000351175.4:p.Ser132=
ENST00000358664.8:c.423C>T ENSP00000351490.4:p.Ser141=
ENST00000394606.6:c.*196C>T ENSP00000378104.2:n.*196C>T
ENST00000553928.5:c.*212C>T ENSP00000451907.1:n.*212C>T
ENST00000555419.5:c.315C>T ENSP00000452405.1:p.Ser105=
ENST00000555932.5:c.164C>T ENSP00000450763.1:p.Ala55Val
ENST00000557277.5:c.234C>T ENSP00000450955.1:p.Ser78=
ENST00000618858.4:c.*212C>T ENSP00000480127.1:n.*212C>T
NM_001271069.1:c.144+17172C>T NP_001257998.1:n.144+17172C>T
NM_002382.4:c.423C>T NP_002373.3:p.Ser141=
NM_145112.2:c.396C>T NP_660087.1:p.Ser132=
NM_145113.2:c.*212C>T NP_660088.1:n.*212C>T
NM_197957.3:c.171+17172C>T NP_932061.1:n.171+17172C>T
NR_073137.1:n.547C>T
XR_429315.2:n.710C>T
NM_001320415.1:c.234C>T NP_001307344.1:p.Ser78=
XM_017021312.2:c.234C>T XP_016876801.1:p.Ser78=
XM_017021313.1:c.234C>T XP_016876802.1:p.Ser78=
XR_001750326.2:n.768C>T
XR_001750327.2:n.687C>T
XR_002957553.1:n.1201C>T
XR_943450.3:n.791C>T
XR_943451.3:n.807C>T
XR_943452.3:n.752C>T
NM_001320415.2:c.234C>T NP_001307344.1:p.Ser78=
NM_002382.5:c.423C>T MANE Select NP_002373.3:p.Ser141=
NM_145112.3:c.396C>T NP_660087.1:p.Ser132=
NM_145113.3:c.*212C>T NP_660088.1:n.*212C>T
NM_001271069.2:c.144+17172C>T NP_001257998.1:n.144+17172C>T
NM_197957.4:c.171+17172C>T NP_932061.1:n.171+17172C>T