Canonical Allele Identifier: CA2625288971

Gene: MAX

Linked Data

• gnomAD v4: 14-65075450-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075450C>G , CM000676.2:g.65075450C>G	GRCh38
NC_000014.8:g.65542168C>G , CM000676.1:g.65542168C>G	GRCh37
NC_000014.7:g.64611921C>G	NCBI36
NG_029830.1:g.32060G>C , LRG_530:g.32060G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*1962G>C	ENSP00000452378.1:n.*1962G>C
ENST00000358664.9:c.*1026G>C MANE Select	ENSP00000351490.4:n.*1026G>C
ENST00000651648.1:c.145-5081G>C	ENSP00000498863.1:n.145-5081G>C
ENST00000284165.10:c.*2353G>C	ENSP00000284165.6:n.*2353G>C
ENST00000341653.6:c.171+18258G>C	ENSP00000342482.2:n.171+18258G>C
ENST00000358402.8:c.*1026G>C	ENSP00000351175.4:n.*1026G>C
ENST00000394606.6:c.*1282G>C	ENSP00000378104.2:n.*1282G>C
ENST00000555932.5:c.*1001G>C	ENSP00000450763.1:n.*1001G>C
ENST00000618858.4:c.*1298G>C	ENSP00000480127.1:n.*1298G>C
NM_001271069.1:c.144+18258G>C	NP_001257998.1:n.144+18258G>C
NM_002382.4:c.*1026G>C	NP_002373.3:n.*1026G>C
NM_145112.2:c.*1026G>C	NP_660087.1:n.*1026G>C
NM_145113.2:c.*1298G>C	NP_660088.1:n.*1298G>C
NM_197957.3:c.171+18258G>C	NP_932061.1:n.171+18258G>C
NR_073137.1:n.1633G>C
XR_429315.2:n.1796G>C
NM_001320415.1:c.*1026G>C	NP_001307344.1:n.*1026G>C
XM_017021312.2:c.*1026G>C	XP_016876801.1:n.*1026G>C
XM_017021313.1:c.*1026G>C	XP_016876802.1:n.*1026G>C
XR_001750326.2:n.1854G>C
XR_001750327.2:n.1773G>C
XR_002957553.1:n.2287G>C
XR_943450.3:n.1877G>C
XR_943451.3:n.1893G>C
XR_943452.3:n.1838G>C
NM_001320415.2:c.*1026G>C	NP_001307344.1:n.*1026G>C
NM_002382.5:c.*1026G>C MANE Select	NP_002373.3:n.*1026G>C
NM_145112.3:c.*1026G>C	NP_660087.1:n.*1026G>C
NM_145113.3:c.*1298G>C	NP_660088.1:n.*1298G>C
NM_001271069.2:c.144+18258G>C	NP_001257998.1:n.144+18258G>C
NM_197957.4:c.171+18258G>C	NP_932061.1:n.171+18258G>C