Canonical Allele Identifier: CA390031824

Gene: MAX

Linked Data

• MyVariant Identifiers: chr14:g.65543328A>T (hg19) ; chr14:g.65076610A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076610A>T , CM000676.2:g.65076610A>T	GRCh38
NC_000014.8:g.65543328A>T , CM000676.1:g.65543328A>T	GRCh37
NC_000014.7:g.64613081A>T	NCBI36
NG_029830.1:g.30900T>A , LRG_530:g.30900T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.130T>A	ENSP00000452206.2:p.Ser44Thr
ENST00000556979.6:c.*802T>A	ENSP00000452378.1:n.*802T>A
ENST00000358664.9:c.349T>A MANE Select	ENSP00000351490.4:p.Ser117Thr
ENST00000651648.1:c.145-6241T>A	ENSP00000498863.1:n.145-6241T>A
ENST00000284165.10:c.*1193T>A	ENSP00000284165.6:n.*1193T>A
ENST00000341653.6:c.171+17098T>A	ENSP00000342482.2:n.171+17098T>A
ENST00000358402.8:c.322T>A	ENSP00000351175.4:p.Ser108Thr
ENST00000358664.8:c.349T>A	ENSP00000351490.4:p.Ser117Thr
ENST00000394606.6:c.*122T>A	ENSP00000378104.2:n.*122T>A
ENST00000553928.5:c.*138T>A	ENSP00000451907.1:n.*138T>A
ENST00000555419.5:c.241T>A	ENSP00000452405.1:p.Ser81Thr
ENST00000555932.5:c.90T>A	ENSP00000450763.1:p.Pro30=
ENST00000556892.5:c.130T>A
ENST00000557277.5:c.160T>A	ENSP00000450955.1:p.Ser54Thr
ENST00000618858.4:c.*138T>A	ENSP00000480127.1:n.*138T>A
NM_001271069.1:c.144+17098T>A	NP_001257998.1:n.144+17098T>A
NM_002382.4:c.349T>A	NP_002373.3:p.Ser117Thr
NM_145112.2:c.322T>A	NP_660087.1:p.Ser108Thr
NM_145113.2:c.*138T>A	NP_660088.1:n.*138T>A
NM_197957.3:c.171+17098T>A	NP_932061.1:n.171+17098T>A
NR_073137.1:n.473T>A
XR_429315.2:n.636T>A
XR_943450.1:n.717T>A
XR_943451.1:n.733T>A
XR_943452.1:n.679T>A
NM_001320415.1:c.160T>A	NP_001307344.1:p.Ser54Thr
XM_017021312.2:c.160T>A	XP_016876801.1:p.Ser54Thr
XM_017021313.1:c.160T>A	XP_016876802.1:p.Ser54Thr
XR_001750326.2:n.694T>A
XR_001750327.2:n.613T>A
XR_002957553.1:n.1127T>A
XR_943450.3:n.717T>A
XR_943451.3:n.733T>A
XR_943452.3:n.678T>A
NM_001320415.2:c.160T>A	NP_001307344.1:p.Ser54Thr
NM_002382.5:c.349T>A MANE Select	NP_002373.3:p.Ser117Thr
NM_145112.3:c.322T>A	NP_660087.1:p.Ser108Thr
NM_145113.3:c.*138T>A	NP_660088.1:n.*138T>A
NM_001271069.2:c.144+17098T>A	NP_001257998.1:n.144+17098T>A
NM_197957.4:c.171+17098T>A	NP_932061.1:n.171+17098T>A