Canonical Allele Identifier: CA390031406

Gene: MAX

Linked Data

• MyVariant Identifiers: chr14:g.65543252G>T (hg19) ; chr14:g.65076534G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076534G>T , CM000676.2:g.65076534G>T	GRCh38
NC_000014.8:g.65543252G>T , CM000676.1:g.65543252G>T	GRCh37
NC_000014.7:g.64613005G>T	NCBI36
NG_029830.1:g.30976C>A , LRG_530:g.30976C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.206C>A	ENSP00000452206.2:p.Ser69Ter
ENST00000556979.6:c.*878C>A	ENSP00000452378.1:n.*878C>A
ENST00000358664.9:c.425C>A MANE Select	ENSP00000351490.4:p.Ser142Ter
ENST00000651648.1:c.145-6165C>A	ENSP00000498863.1:n.145-6165C>A
ENST00000284165.10:c.*1269C>A	ENSP00000284165.6:n.*1269C>A
ENST00000341653.6:c.171+17174C>A	ENSP00000342482.2:n.171+17174C>A
ENST00000358402.8:c.398C>A	ENSP00000351175.4:p.Ser133Ter
ENST00000358664.8:c.425C>A	ENSP00000351490.4:p.Ser142Ter
ENST00000394606.6:c.*198C>A	ENSP00000378104.2:n.*198C>A
ENST00000553928.5:c.*214C>A	ENSP00000451907.1:n.*214C>A
ENST00000555419.5:c.317C>A	ENSP00000452405.1:p.Ser106Ter
ENST00000555932.5:c.166C>A	ENSP00000450763.1:p.Arg56=
ENST00000557277.5:c.236C>A	ENSP00000450955.1:p.Ser79Ter
ENST00000618858.4:c.*214C>A	ENSP00000480127.1:n.*214C>A
NM_001271069.1:c.144+17174C>A	NP_001257998.1:n.144+17174C>A
NM_002382.4:c.425C>A	NP_002373.3:p.Ser142Ter
NM_145112.2:c.398C>A	NP_660087.1:p.Ser133Ter
NM_145113.2:c.*214C>A	NP_660088.1:n.*214C>A
NM_197957.3:c.171+17174C>A	NP_932061.1:n.171+17174C>A
NR_073137.1:n.549C>A
XR_429315.2:n.712C>A
NM_001320415.1:c.236C>A	NP_001307344.1:p.Ser79Ter
XM_017021312.2:c.236C>A	XP_016876801.1:p.Ser79Ter
XM_017021313.1:c.236C>A	XP_016876802.1:p.Ser79Ter
XR_001750326.2:n.770C>A
XR_001750327.2:n.689C>A
XR_002957553.1:n.1203C>A
XR_943450.3:n.793C>A
XR_943451.3:n.809C>A
XR_943452.3:n.754C>A
NM_001320415.2:c.236C>A	NP_001307344.1:p.Ser79Ter
NM_002382.5:c.425C>A MANE Select	NP_002373.3:p.Ser142Ter
NM_145112.3:c.398C>A	NP_660087.1:p.Ser133Ter
NM_145113.3:c.*214C>A	NP_660088.1:n.*214C>A
NM_001271069.2:c.144+17174C>A	NP_001257998.1:n.144+17174C>A
NM_197957.4:c.171+17174C>A	NP_932061.1:n.171+17174C>A