Canonical Allele Identifier: CA2625288829

Gene: MAX

Linked Data

• gnomAD v4: 14-65075227-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075227C>A , CM000676.2:g.65075227C>A	GRCh38
NC_000014.8:g.65541945C>A , CM000676.1:g.65541945C>A	GRCh37
NC_000014.7:g.64611698C>A	NCBI36
NG_029830.1:g.32283G>T , LRG_530:g.32283G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*2185G>T	ENSP00000452378.1:n.*2185G>T
ENST00000358664.9:c.*1249G>T MANE Select	ENSP00000351490.4:n.*1249G>T
ENST00000651648.1:c.145-4858G>T	ENSP00000498863.1:n.145-4858G>T
ENST00000284165.10:c.*2576G>T	ENSP00000284165.6:n.*2576G>T
ENST00000341653.6:c.171+18481G>T	ENSP00000342482.2:n.171+18481G>T
ENST00000358402.8:c.*1249G>T	ENSP00000351175.4:n.*1249G>T
ENST00000394606.6:c.*1505G>T	ENSP00000378104.2:n.*1505G>T
ENST00000555932.5:c.*1224G>T	ENSP00000450763.1:n.*1224G>T
ENST00000618858.4:c.*1521G>T	ENSP00000480127.1:n.*1521G>T
NM_001271069.1:c.144+18481G>T	NP_001257998.1:n.144+18481G>T
NM_002382.4:c.*1249G>T	NP_002373.3:n.*1249G>T
NM_145112.2:c.*1249G>T	NP_660087.1:n.*1249G>T
NM_145113.2:c.*1521G>T	NP_660088.1:n.*1521G>T
NM_197957.3:c.171+18481G>T	NP_932061.1:n.171+18481G>T
NR_073137.1:n.1856G>T
XR_429315.2:n.2019G>T
NM_001320415.1:c.*1249G>T	NP_001307344.1:n.*1249G>T
XM_017021312.2:c.*1249G>T	XP_016876801.1:n.*1249G>T
XM_017021313.1:c.*1249G>T	XP_016876802.1:n.*1249G>T
XR_001750326.2:n.2077G>T
XR_001750327.2:n.1996G>T
XR_002957553.1:n.2510G>T
XR_943450.3:n.2100G>T
XR_943451.3:n.2116G>T
XR_943452.3:n.2061G>T
NM_001320415.2:c.*1249G>T	NP_001307344.1:n.*1249G>T
NM_002382.5:c.*1249G>T MANE Select	NP_002373.3:n.*1249G>T
NM_145112.3:c.*1249G>T	NP_660087.1:n.*1249G>T
NM_145113.3:c.*1521G>T	NP_660088.1:n.*1521G>T
NM_001271069.2:c.144+18481G>T	NP_001257998.1:n.144+18481G>T
NM_197957.4:c.171+18481G>T	NP_932061.1:n.171+18481G>T