Canonical Allele Identifier: CA390031593

Gene: MAX

Linked Data

• MyVariant Identifiers: chr14:g.65543282G>T (hg19) ; chr14:g.65076564G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076564G>T , CM000676.2:g.65076564G>T	GRCh38
NC_000014.8:g.65543282G>T , CM000676.1:g.65543282G>T	GRCh37
NC_000014.7:g.64613035G>T	NCBI36
NG_029830.1:g.30946C>A , LRG_530:g.30946C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.176C>A	ENSP00000452206.2:p.Ser59Tyr
ENST00000556979.6:c.*848C>A	ENSP00000452378.1:n.*848C>A
ENST00000358664.9:c.395C>A MANE Select	ENSP00000351490.4:p.Ser132Tyr
ENST00000651648.1:c.145-6195C>A	ENSP00000498863.1:n.145-6195C>A
ENST00000284165.10:c.*1239C>A	ENSP00000284165.6:n.*1239C>A
ENST00000341653.6:c.171+17144C>A	ENSP00000342482.2:n.171+17144C>A
ENST00000358402.8:c.368C>A	ENSP00000351175.4:p.Ser123Tyr
ENST00000358664.8:c.395C>A	ENSP00000351490.4:p.Ser132Tyr
ENST00000394606.6:c.*168C>A	ENSP00000378104.2:n.*168C>A
ENST00000553928.5:c.*184C>A	ENSP00000451907.1:n.*184C>A
ENST00000555419.5:c.287C>A	ENSP00000452405.1:p.Ser96Tyr
ENST00000555932.5:c.136C>A	ENSP00000450763.1:p.Leu46Met
ENST00000557277.5:c.206C>A	ENSP00000450955.1:p.Ser69Tyr
ENST00000618858.4:c.*184C>A	ENSP00000480127.1:n.*184C>A
NM_001271069.1:c.144+17144C>A	NP_001257998.1:n.144+17144C>A
NM_002382.4:c.395C>A	NP_002373.3:p.Ser132Tyr
NM_145112.2:c.368C>A	NP_660087.1:p.Ser123Tyr
NM_145113.2:c.*184C>A	NP_660088.1:n.*184C>A
NM_197957.3:c.171+17144C>A	NP_932061.1:n.171+17144C>A
NR_073137.1:n.519C>A
XR_429315.2:n.682C>A
NM_001320415.1:c.206C>A	NP_001307344.1:p.Ser69Tyr
XM_017021312.2:c.206C>A	XP_016876801.1:p.Ser69Tyr
XM_017021313.1:c.206C>A	XP_016876802.1:p.Ser69Tyr
XR_001750326.2:n.740C>A
XR_001750327.2:n.659C>A
XR_002957553.1:n.1173C>A
XR_943450.3:n.763C>A
XR_943451.3:n.779C>A
XR_943452.3:n.724C>A
NM_001320415.2:c.206C>A	NP_001307344.1:p.Ser69Tyr
NM_002382.5:c.395C>A MANE Select	NP_002373.3:p.Ser132Tyr
NM_145112.3:c.368C>A	NP_660087.1:p.Ser123Tyr
NM_145113.3:c.*184C>A	NP_660088.1:n.*184C>A
NM_001271069.2:c.144+17144C>A	NP_001257998.1:n.144+17144C>A
NM_197957.4:c.171+17144C>A	NP_932061.1:n.171+17144C>A