Canonical Allele Identifier: CA2625289527

Gene: MAX

Linked Data

• gnomAD v4: 14-65076095-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076095G>T , CM000676.2:g.65076095G>T	GRCh38
NC_000014.8:g.65542813G>T , CM000676.1:g.65542813G>T	GRCh37
NC_000014.7:g.64612566G>T	NCBI36
NG_029830.1:g.31415C>A , LRG_530:g.31415C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*381C>A	ENSP00000452206.2:n.*381C>A
ENST00000556979.6:c.*1317C>A	ENSP00000452378.1:n.*1317C>A
ENST00000358664.9:c.*381C>A MANE Select	ENSP00000351490.4:n.*381C>A
ENST00000651648.1:c.145-5726C>A	ENSP00000498863.1:n.145-5726C>A
ENST00000284165.10:c.*1708C>A	ENSP00000284165.6:n.*1708C>A
ENST00000341653.6:c.171+17613C>A	ENSP00000342482.2:n.171+17613C>A
ENST00000358402.8:c.*381C>A	ENSP00000351175.4:n.*381C>A
ENST00000358664.8:c.*381C>A	ENSP00000351490.4:n.*381C>A
ENST00000394606.6:c.*637C>A	ENSP00000378104.2:n.*637C>A
ENST00000555419.5:c.756C>A	ENSP00000452405.1:n.756C>A
ENST00000555932.5:c.*356C>A	ENSP00000450763.1:n.*356C>A
ENST00000618858.4:c.*653C>A	ENSP00000480127.1:n.*653C>A
NM_001271069.1:c.144+17613C>A	NP_001257998.1:n.144+17613C>A
NM_002382.4:c.*381C>A	NP_002373.3:n.*381C>A
NM_145112.2:c.*381C>A	NP_660087.1:n.*381C>A
NM_145113.2:c.*653C>A	NP_660088.1:n.*653C>A
NM_197957.3:c.171+17613C>A	NP_932061.1:n.171+17613C>A
NR_073137.1:n.988C>A
XR_429315.2:n.1151C>A
NM_001320415.1:c.*381C>A	NP_001307344.1:n.*381C>A
XM_017021312.2:c.*381C>A	XP_016876801.1:n.*381C>A
XM_017021313.1:c.*381C>A	XP_016876802.1:n.*381C>A
XR_001750326.2:n.1209C>A
XR_001750327.2:n.1128C>A
XR_002957553.1:n.1642C>A
XR_943450.3:n.1232C>A
XR_943451.3:n.1248C>A
XR_943452.3:n.1193C>A
NM_001320415.2:c.*381C>A	NP_001307344.1:n.*381C>A
NM_002382.5:c.*381C>A MANE Select	NP_002373.3:n.*381C>A
NM_145112.3:c.*381C>A	NP_660087.1:n.*381C>A
NM_145113.3:c.*653C>A	NP_660088.1:n.*653C>A
NM_001271069.2:c.144+17613C>A	NP_001257998.1:n.144+17613C>A
NM_197957.4:c.171+17613C>A	NP_932061.1:n.171+17613C>A