Canonical Allele Identifier: CA390031569

Gene: MAX

Linked Data

• MyVariant Identifiers: chr14:g.65543279G>T (hg19) ; chr14:g.65076561G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076561G>T , CM000676.2:g.65076561G>T	GRCh38
NC_000014.8:g.65543279G>T , CM000676.1:g.65543279G>T	GRCh37
NC_000014.7:g.64613032G>T	NCBI36
NG_029830.1:g.30949C>A , LRG_530:g.30949C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.179C>A	ENSP00000452206.2:p.Ala60Asp
ENST00000556979.6:c.*851C>A	ENSP00000452378.1:n.*851C>A
ENST00000358664.9:c.398C>A MANE Select	ENSP00000351490.4:p.Ala133Asp
ENST00000651648.1:c.145-6192C>A	ENSP00000498863.1:n.145-6192C>A
ENST00000284165.10:c.*1242C>A	ENSP00000284165.6:n.*1242C>A
ENST00000341653.6:c.171+17147C>A	ENSP00000342482.2:n.171+17147C>A
ENST00000358402.8:c.371C>A	ENSP00000351175.4:p.Ala124Asp
ENST00000358664.8:c.398C>A	ENSP00000351490.4:p.Ala133Asp
ENST00000394606.6:c.*171C>A	ENSP00000378104.2:n.*171C>A
ENST00000553928.5:c.*187C>A	ENSP00000451907.1:n.*187C>A
ENST00000555419.5:c.290C>A	ENSP00000452405.1:p.Ala97Asp
ENST00000555932.5:c.139C>A	ENSP00000450763.1:p.Pro47Thr
ENST00000557277.5:c.209C>A	ENSP00000450955.1:p.Ala70Asp
ENST00000618858.4:c.*187C>A	ENSP00000480127.1:n.*187C>A
NM_001271069.1:c.144+17147C>A	NP_001257998.1:n.144+17147C>A
NM_002382.4:c.398C>A	NP_002373.3:p.Ala133Asp
NM_145112.2:c.371C>A	NP_660087.1:p.Ala124Asp
NM_145113.2:c.*187C>A	NP_660088.1:n.*187C>A
NM_197957.3:c.171+17147C>A	NP_932061.1:n.171+17147C>A
NR_073137.1:n.522C>A
XR_429315.2:n.685C>A
NM_001320415.1:c.209C>A	NP_001307344.1:p.Ala70Asp
XM_017021312.2:c.209C>A	XP_016876801.1:p.Ala70Asp
XM_017021313.1:c.209C>A	XP_016876802.1:p.Ala70Asp
XR_001750326.2:n.743C>A
XR_001750327.2:n.662C>A
XR_002957553.1:n.1176C>A
XR_943450.3:n.766C>A
XR_943451.3:n.782C>A
XR_943452.3:n.727C>A
NM_001320415.2:c.209C>A	NP_001307344.1:p.Ala70Asp
NM_002382.5:c.398C>A MANE Select	NP_002373.3:p.Ala133Asp
NM_145112.3:c.371C>A	NP_660087.1:p.Ala124Asp
NM_145113.3:c.*187C>A	NP_660088.1:n.*187C>A
NM_001271069.2:c.144+17147C>A	NP_001257998.1:n.144+17147C>A
NM_197957.4:c.171+17147C>A	NP_932061.1:n.171+17147C>A