Canonical Allele Identifier: CA2625288933

Gene: MAX

Linked Data

• gnomAD v4: 14-65075397-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075397A>G , CM000676.2:g.65075397A>G	GRCh38
NC_000014.8:g.65542115A>G , CM000676.1:g.65542115A>G	GRCh37
NC_000014.7:g.64611868A>G	NCBI36
NG_029830.1:g.32113T>C , LRG_530:g.32113T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*2015T>C	ENSP00000452378.1:n.*2015T>C
ENST00000358664.9:c.*1079T>C MANE Select	ENSP00000351490.4:n.*1079T>C
ENST00000651648.1:c.145-5028T>C	ENSP00000498863.1:n.145-5028T>C
ENST00000284165.10:c.*2406T>C	ENSP00000284165.6:n.*2406T>C
ENST00000341653.6:c.171+18311T>C	ENSP00000342482.2:n.171+18311T>C
ENST00000358402.8:c.*1079T>C	ENSP00000351175.4:n.*1079T>C
ENST00000394606.6:c.*1335T>C	ENSP00000378104.2:n.*1335T>C
ENST00000555932.5:c.*1054T>C	ENSP00000450763.1:n.*1054T>C
ENST00000618858.4:c.*1351T>C	ENSP00000480127.1:n.*1351T>C
NM_001271069.1:c.144+18311T>C	NP_001257998.1:n.144+18311T>C
NM_002382.4:c.*1079T>C	NP_002373.3:n.*1079T>C
NM_145112.2:c.*1079T>C	NP_660087.1:n.*1079T>C
NM_145113.2:c.*1351T>C	NP_660088.1:n.*1351T>C
NM_197957.3:c.171+18311T>C	NP_932061.1:n.171+18311T>C
NR_073137.1:n.1686T>C
XR_429315.2:n.1849T>C
NM_001320415.1:c.*1079T>C	NP_001307344.1:n.*1079T>C
XM_017021312.2:c.*1079T>C	XP_016876801.1:n.*1079T>C
XM_017021313.1:c.*1079T>C	XP_016876802.1:n.*1079T>C
XR_001750326.2:n.1907T>C
XR_001750327.2:n.1826T>C
XR_002957553.1:n.2340T>C
XR_943450.3:n.1930T>C
XR_943451.3:n.1946T>C
XR_943452.3:n.1891T>C
NM_001320415.2:c.*1079T>C	NP_001307344.1:n.*1079T>C
NM_002382.5:c.*1079T>C MANE Select	NP_002373.3:n.*1079T>C
NM_145112.3:c.*1079T>C	NP_660087.1:n.*1079T>C
NM_145113.3:c.*1351T>C	NP_660088.1:n.*1351T>C
NM_001271069.2:c.144+18311T>C	NP_001257998.1:n.144+18311T>C
NM_197957.4:c.171+18311T>C	NP_932061.1:n.171+18311T>C