Canonical Allele Identifier: CA2729722857

Gene: MAX

Linked Data

• dbSNP Id: rs2139738059

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076402C>T , CM000676.2:g.65076402C>T	GRCh38
NC_000014.8:g.65543120C>T , CM000676.1:g.65543120C>T	GRCh37
NC_000014.7:g.64612873C>T	NCBI36
NG_029830.1:g.31108G>A , LRG_530:g.31108G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*74G>A	ENSP00000452206.2:n.*74G>A
ENST00000556979.6:c.*1010G>A	ENSP00000452378.1:n.*1010G>A
ENST00000358664.9:c.*74G>A MANE Select	ENSP00000351490.4:n.*74G>A
ENST00000651648.1:c.145-6033G>A	ENSP00000498863.1:n.145-6033G>A
ENST00000284165.10:c.*1401G>A	ENSP00000284165.6:n.*1401G>A
ENST00000341653.6:c.171+17306G>A	ENSP00000342482.2:n.171+17306G>A
ENST00000358402.8:c.*74G>A	ENSP00000351175.4:n.*74G>A
ENST00000358664.8:c.*74G>A	ENSP00000351490.4:n.*74G>A
ENST00000394606.6:c.*330G>A	ENSP00000378104.2:n.*330G>A
ENST00000555419.5:c.449G>A	ENSP00000452405.1:n.449G>A
ENST00000555932.5:c.*49G>A	ENSP00000450763.1:n.*49G>A
ENST00000618858.4:c.*346G>A	ENSP00000480127.1:n.*346G>A
NM_001271069.1:c.144+17306G>A	NP_001257998.1:n.144+17306G>A
NM_002382.4:c.*74G>A	NP_002373.3:n.*74G>A
NM_145112.2:c.*74G>A	NP_660087.1:n.*74G>A
NM_145113.2:c.*346G>A	NP_660088.1:n.*346G>A
NM_197957.3:c.171+17306G>A	NP_932061.1:n.171+17306G>A
NR_073137.1:n.681G>A
XR_429315.2:n.844G>A
NM_001320415.1:c.*74G>A	NP_001307344.1:n.*74G>A
XM_017021312.2:c.*74G>A	XP_016876801.1:n.*74G>A
XM_017021313.1:c.*74G>A	XP_016876802.1:n.*74G>A
XR_001750326.2:n.902G>A
XR_001750327.2:n.821G>A
XR_002957553.1:n.1335G>A
XR_943450.3:n.925G>A
XR_943451.3:n.941G>A
XR_943452.3:n.886G>A
NM_001320415.2:c.*74G>A	NP_001307344.1:n.*74G>A
NM_002382.5:c.*74G>A MANE Select	NP_002373.3:n.*74G>A
NM_145112.3:c.*74G>A	NP_660087.1:n.*74G>A
NM_145113.3:c.*346G>A	NP_660088.1:n.*346G>A
NM_001271069.2:c.144+17306G>A	NP_001257998.1:n.144+17306G>A
NM_197957.4:c.171+17306G>A	NP_932061.1:n.171+17306G>A