Canonical Allele Identifier: CA262716763

Gene: MAX

Linked Data

• dbSNP Id: rs576515287
• gnomAD v3: 14-65076086-C-A
• gnomAD v4: 14-65076086-C-A
• MyVariant Identifiers: chr14:g.65542804C>A (hg19) ; chr14:g.65076086C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076086C>A , CM000676.2:g.65076086C>A	GRCh38
NC_000014.8:g.65542804C>A , CM000676.1:g.65542804C>A	GRCh37
NC_000014.7:g.64612557C>A	NCBI36
NG_029830.1:g.31424G>T , LRG_530:g.31424G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*390G>T	ENSP00000452206.2:n.*390G>T
ENST00000556979.6:c.*1326G>T	ENSP00000452378.1:n.*1326G>T
ENST00000358664.9:c.*390G>T MANE Select	ENSP00000351490.4:n.*390G>T
ENST00000651648.1:c.145-5717G>T	ENSP00000498863.1:n.145-5717G>T
ENST00000284165.10:c.*1717G>T	ENSP00000284165.6:n.*1717G>T
ENST00000341653.6:c.171+17622G>T	ENSP00000342482.2:n.171+17622G>T
ENST00000358402.8:c.*390G>T	ENSP00000351175.4:n.*390G>T
ENST00000358664.8:c.*390G>T	ENSP00000351490.4:n.*390G>T
ENST00000394606.6:c.*646G>T	ENSP00000378104.2:n.*646G>T
ENST00000555419.5:c.765G>T	ENSP00000452405.1:n.765G>T
ENST00000555932.5:c.*365G>T	ENSP00000450763.1:n.*365G>T
ENST00000618858.4:c.*662G>T	ENSP00000480127.1:n.*662G>T
NM_001271069.1:c.144+17622G>T	NP_001257998.1:n.144+17622G>T
NM_002382.4:c.*390G>T	NP_002373.3:n.*390G>T
NM_145112.2:c.*390G>T	NP_660087.1:n.*390G>T
NM_145113.2:c.*662G>T	NP_660088.1:n.*662G>T
NM_197957.3:c.171+17622G>T	NP_932061.1:n.171+17622G>T
NR_073137.1:n.997G>T
XR_429315.2:n.1160G>T
NM_001320415.1:c.*390G>T	NP_001307344.1:n.*390G>T
XM_017021312.2:c.*390G>T	XP_016876801.1:n.*390G>T
XM_017021313.1:c.*390G>T	XP_016876802.1:n.*390G>T
XR_001750326.2:n.1218G>T
XR_001750327.2:n.1137G>T
XR_002957553.1:n.1651G>T
XR_943450.3:n.1241G>T
XR_943451.3:n.1257G>T
XR_943452.3:n.1202G>T
NM_001320415.2:c.*390G>T	NP_001307344.1:n.*390G>T
NM_002382.5:c.*390G>T MANE Select	NP_002373.3:n.*390G>T
NM_145112.3:c.*390G>T	NP_660087.1:n.*390G>T
NM_145113.3:c.*662G>T	NP_660088.1:n.*662G>T
NM_001271069.2:c.144+17622G>T	NP_001257998.1:n.144+17622G>T
NM_197957.4:c.171+17622G>T	NP_932061.1:n.171+17622G>T