Canonical Allele Identifier: CA390031432

Gene: MAX

Linked Data

• gnomAD v4: 14-65076540-G-A
• MyVariant Identifiers: chr14:g.65543258G>A (hg19) ; chr14:g.65076540G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076540G>A , CM000676.2:g.65076540G>A	GRCh38
NC_000014.8:g.65543258G>A , CM000676.1:g.65543258G>A	GRCh37
NC_000014.7:g.64613011G>A	NCBI36
NG_029830.1:g.30970C>T , LRG_530:g.30970C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.200C>T	ENSP00000452206.2:p.Ser67Phe
ENST00000556979.6:c.*872C>T	ENSP00000452378.1:n.*872C>T
ENST00000358664.9:c.419C>T MANE Select	ENSP00000351490.4:p.Ser140Phe
ENST00000651648.1:c.145-6171C>T	ENSP00000498863.1:n.145-6171C>T
ENST00000284165.10:c.*1263C>T	ENSP00000284165.6:n.*1263C>T
ENST00000341653.6:c.171+17168C>T	ENSP00000342482.2:n.171+17168C>T
ENST00000358402.8:c.392C>T	ENSP00000351175.4:p.Ser131Phe
ENST00000358664.8:c.419C>T	ENSP00000351490.4:p.Ser140Phe
ENST00000394606.6:c.*192C>T	ENSP00000378104.2:n.*192C>T
ENST00000553928.5:c.*208C>T	ENSP00000451907.1:n.*208C>T
ENST00000555419.5:c.311C>T	ENSP00000452405.1:p.Ser104Phe
ENST00000555932.5:c.160C>T	ENSP00000450763.1:p.Pro54Ser
ENST00000557277.5:c.230C>T	ENSP00000450955.1:p.Ser77Phe
ENST00000618858.4:c.*208C>T	ENSP00000480127.1:n.*208C>T
NM_001271069.1:c.144+17168C>T	NP_001257998.1:n.144+17168C>T
NM_002382.4:c.419C>T	NP_002373.3:p.Ser140Phe
NM_145112.2:c.392C>T	NP_660087.1:p.Ser131Phe
NM_145113.2:c.*208C>T	NP_660088.1:n.*208C>T
NM_197957.3:c.171+17168C>T	NP_932061.1:n.171+17168C>T
NR_073137.1:n.543C>T
XR_429315.2:n.706C>T
NM_001320415.1:c.230C>T	NP_001307344.1:p.Ser77Phe
XM_017021312.2:c.230C>T	XP_016876801.1:p.Ser77Phe
XM_017021313.1:c.230C>T	XP_016876802.1:p.Ser77Phe
XR_001750326.2:n.764C>T
XR_001750327.2:n.683C>T
XR_002957553.1:n.1197C>T
XR_943450.3:n.787C>T
XR_943451.3:n.803C>T
XR_943452.3:n.748C>T
NM_001320415.2:c.230C>T	NP_001307344.1:p.Ser77Phe
NM_002382.5:c.419C>T MANE Select	NP_002373.3:p.Ser140Phe
NM_145112.3:c.392C>T	NP_660087.1:p.Ser131Phe
NM_145113.3:c.*208C>T	NP_660088.1:n.*208C>T
NM_001271069.2:c.144+17168C>T	NP_001257998.1:n.144+17168C>T
NM_197957.4:c.171+17168C>T	NP_932061.1:n.171+17168C>T