Canonical Allele Identifier: CA2625289579

Gene: MAX

Linked Data

• gnomAD v4: 14-65076129-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076131del , CM000676.2:g.65076131del	GRCh38
NC_000014.8:g.65542849del , CM000676.1:g.65542849del	GRCh37
NC_000014.7:g.64612602del	NCBI36
NG_029830.1:g.31380del , LRG_530:g.31380del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*346del	ENSP00000452206.2:n.*346del
ENST00000556979.6:c.*1282del	ENSP00000452378.1:n.*1282del
ENST00000358664.9:c.*346del MANE Select	ENSP00000351490.4:n.*346del
ENST00000651648.1:c.145-5761del	ENSP00000498863.1:n.145-5761del
ENST00000284165.10:c.*1673del	ENSP00000284165.6:n.*1673del
ENST00000341653.6:c.171+17578del	ENSP00000342482.2:n.171+17578del
ENST00000358402.8:c.*346del	ENSP00000351175.4:n.*346del
ENST00000358664.8:c.*346del	ENSP00000351490.4:n.*346del
ENST00000394606.6:c.*602del	ENSP00000378104.2:n.*602del
ENST00000555419.5:c.721del	ENSP00000452405.1:n.721del
ENST00000555932.5:c.*321del	ENSP00000450763.1:n.*321del
ENST00000618858.4:c.*618del	ENSP00000480127.1:n.*618del
NM_001271069.1:c.144+17578del	NP_001257998.1:n.144+17578del
NM_002382.4:c.*346del	NP_002373.3:n.*346del
NM_145112.2:c.*346del	NP_660087.1:n.*346del
NM_145113.2:c.*618del	NP_660088.1:n.*618del
NM_197957.3:c.171+17578del	NP_932061.1:n.171+17578del
NR_073137.1:n.953del
XR_429315.2:n.1116del
NM_001320415.1:c.*346del	NP_001307344.1:n.*346del
XM_017021312.2:c.*346del	XP_016876801.1:n.*346del
XM_017021313.1:c.*346del	XP_016876802.1:n.*346del
XR_001750326.2:n.1174del
XR_001750327.2:n.1093del
XR_002957553.1:n.1607del
XR_943450.3:n.1197del
XR_943451.3:n.1213del
XR_943452.3:n.1158del
NM_001320415.2:c.*346del	NP_001307344.1:n.*346del
NM_002382.5:c.*346del MANE Select	NP_002373.3:n.*346del
NM_145112.3:c.*346del	NP_660087.1:n.*346del
NM_145113.3:c.*618del	NP_660088.1:n.*618del
NM_001271069.2:c.144+17578del	NP_001257998.1:n.144+17578del
NM_197957.4:c.171+17578del	NP_932061.1:n.171+17578del