Canonical Allele Identifier: CA390031558

Gene: MAX

Linked Data

• MyVariant Identifiers: chr14:g.65543277A>G (hg19) ; chr14:g.65076559A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076559A>G , CM000676.2:g.65076559A>G	GRCh38
NC_000014.8:g.65543277A>G , CM000676.1:g.65543277A>G	GRCh37
NC_000014.7:g.64613030A>G	NCBI36
NG_029830.1:g.30951T>C , LRG_530:g.30951T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.181T>C	ENSP00000452206.2:p.Phe61Leu
ENST00000556979.6:c.*853T>C	ENSP00000452378.1:n.*853T>C
ENST00000358664.9:c.400T>C MANE Select	ENSP00000351490.4:p.Phe134Leu
ENST00000651648.1:c.145-6190T>C	ENSP00000498863.1:n.145-6190T>C
ENST00000284165.10:c.*1244T>C	ENSP00000284165.6:n.*1244T>C
ENST00000341653.6:c.171+17149T>C	ENSP00000342482.2:n.171+17149T>C
ENST00000358402.8:c.373T>C	ENSP00000351175.4:p.Phe125Leu
ENST00000358664.8:c.400T>C	ENSP00000351490.4:p.Phe134Leu
ENST00000394606.6:c.*173T>C	ENSP00000378104.2:n.*173T>C
ENST00000553928.5:c.*189T>C	ENSP00000451907.1:n.*189T>C
ENST00000555419.5:c.292T>C	ENSP00000452405.1:p.Phe98Leu
ENST00000555932.5:c.141T>C	ENSP00000450763.1:p.Pro47=
ENST00000557277.5:c.211T>C	ENSP00000450955.1:p.Phe71Leu
ENST00000618858.4:c.*189T>C	ENSP00000480127.1:n.*189T>C
NM_001271069.1:c.144+17149T>C	NP_001257998.1:n.144+17149T>C
NM_002382.4:c.400T>C	NP_002373.3:p.Phe134Leu
NM_145112.2:c.373T>C	NP_660087.1:p.Phe125Leu
NM_145113.2:c.*189T>C	NP_660088.1:n.*189T>C
NM_197957.3:c.171+17149T>C	NP_932061.1:n.171+17149T>C
NR_073137.1:n.524T>C
XR_429315.2:n.687T>C
NM_001320415.1:c.211T>C	NP_001307344.1:p.Phe71Leu
XM_017021312.2:c.211T>C	XP_016876801.1:p.Phe71Leu
XM_017021313.1:c.211T>C	XP_016876802.1:p.Phe71Leu
XR_001750326.2:n.745T>C
XR_001750327.2:n.664T>C
XR_002957553.1:n.1178T>C
XR_943450.3:n.768T>C
XR_943451.3:n.784T>C
XR_943452.3:n.729T>C
NM_001320415.2:c.211T>C	NP_001307344.1:p.Phe71Leu
NM_002382.5:c.400T>C MANE Select	NP_002373.3:p.Phe134Leu
NM_145112.3:c.373T>C	NP_660087.1:p.Phe125Leu
NM_145113.3:c.*189T>C	NP_660088.1:n.*189T>C
NM_001271069.2:c.144+17149T>C	NP_001257998.1:n.144+17149T>C
NM_197957.4:c.171+17149T>C	NP_932061.1:n.171+17149T>C