Canonical Allele Identifier: CA2625288950

Gene: MAX

Linked Data

• gnomAD v4: 14-65075411-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075412del , CM000676.2:g.65075412del	GRCh38
NC_000014.8:g.65542130del , CM000676.1:g.65542130del	GRCh37
NC_000014.7:g.64611883del	NCBI36
NG_029830.1:g.32098del , LRG_530:g.32098del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*2000del	ENSP00000452378.1:n.*2000del
ENST00000358664.9:c.*1064del MANE Select	ENSP00000351490.4:n.*1064del
ENST00000651648.1:c.145-5043del	ENSP00000498863.1:n.145-5043del
ENST00000284165.10:c.*2391del	ENSP00000284165.6:n.*2391del
ENST00000341653.6:c.171+18296del	ENSP00000342482.2:n.171+18296del
ENST00000358402.8:c.*1064del	ENSP00000351175.4:n.*1064del
ENST00000394606.6:c.*1320del	ENSP00000378104.2:n.*1320del
ENST00000555932.5:c.*1039del	ENSP00000450763.1:n.*1039del
ENST00000618858.4:c.*1336del	ENSP00000480127.1:n.*1336del
NM_001271069.1:c.144+18296del	NP_001257998.1:n.144+18296del
NM_002382.4:c.*1064del	NP_002373.3:n.*1064del
NM_145112.2:c.*1064del	NP_660087.1:n.*1064del
NM_145113.2:c.*1336del	NP_660088.1:n.*1336del
NM_197957.3:c.171+18296del	NP_932061.1:n.171+18296del
NR_073137.1:n.1671del
XR_429315.2:n.1834del
NM_001320415.1:c.*1064del	NP_001307344.1:n.*1064del
XM_017021312.2:c.*1064del	XP_016876801.1:n.*1064del
XM_017021313.1:c.*1064del	XP_016876802.1:n.*1064del
XR_001750326.2:n.1892del
XR_001750327.2:n.1811del
XR_002957553.1:n.2325del
XR_943450.3:n.1915del
XR_943451.3:n.1931del
XR_943452.3:n.1876del
NM_001320415.2:c.*1064del	NP_001307344.1:n.*1064del
NM_002382.5:c.*1064del MANE Select	NP_002373.3:n.*1064del
NM_145112.3:c.*1064del	NP_660087.1:n.*1064del
NM_145113.3:c.*1336del	NP_660088.1:n.*1336del
NM_001271069.2:c.144+18296del	NP_001257998.1:n.144+18296del
NM_197957.4:c.171+18296del	NP_932061.1:n.171+18296del