Canonical Allele Identifier: CA2625289168

Gene: MAX

Linked Data

• gnomAD v4: 14-65075776-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075777del , CM000676.2:g.65075777del	GRCh38
NC_000014.8:g.65542495del , CM000676.1:g.65542495del	GRCh37
NC_000014.7:g.64612248del	NCBI36
NG_029830.1:g.31733del , LRG_530:g.31733del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*699del	ENSP00000452206.2:n.*699del
ENST00000556979.6:c.*1635del	ENSP00000452378.1:n.*1635del
ENST00000358664.9:c.*699del MANE Select	ENSP00000351490.4:n.*699del
ENST00000651648.1:c.145-5408del	ENSP00000498863.1:n.145-5408del
ENST00000284165.10:c.*2026del	ENSP00000284165.6:n.*2026del
ENST00000341653.6:c.171+17931del	ENSP00000342482.2:n.171+17931del
ENST00000358402.8:c.*699del	ENSP00000351175.4:n.*699del
ENST00000358664.8:c.*699del	ENSP00000351490.4:n.*699del
ENST00000394606.6:c.*955del	ENSP00000378104.2:n.*955del
ENST00000555932.5:c.*674del	ENSP00000450763.1:n.*674del
ENST00000618858.4:c.*971del	ENSP00000480127.1:n.*971del
NM_001271069.1:c.144+17931del	NP_001257998.1:n.144+17931del
NM_002382.4:c.*699del	NP_002373.3:n.*699del
NM_145112.2:c.*699del	NP_660087.1:n.*699del
NM_145113.2:c.*971del	NP_660088.1:n.*971del
NM_197957.3:c.171+17931del	NP_932061.1:n.171+17931del
NR_073137.1:n.1306del
XR_429315.2:n.1469del
NM_001320415.1:c.*699del	NP_001307344.1:n.*699del
XM_017021312.2:c.*699del	XP_016876801.1:n.*699del
XM_017021313.1:c.*699del	XP_016876802.1:n.*699del
XR_001750326.2:n.1527del
XR_001750327.2:n.1446del
XR_002957553.1:n.1960del
XR_943450.3:n.1550del
XR_943451.3:n.1566del
XR_943452.3:n.1511del
NM_001320415.2:c.*699del	NP_001307344.1:n.*699del
NM_002382.5:c.*699del MANE Select	NP_002373.3:n.*699del
NM_145112.3:c.*699del	NP_660087.1:n.*699del
NM_145113.3:c.*971del	NP_660088.1:n.*971del
NM_001271069.2:c.144+17931del	NP_001257998.1:n.144+17931del
NM_197957.4:c.171+17931del	NP_932061.1:n.171+17931del