Canonical Allele Identifier: CA2142951306

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075831_65075833delinsTGA , CM000676.2:g.65075831_65075833delinsTGA	GRCh38
NC_000014.8:g.65542549_65542551delinsTGA , CM000676.1:g.65542549_65542551delinsTGA	GRCh37
NC_000014.7:g.64612302_64612304delinsTGA	NCBI36
NG_029830.1:g.31677_31679delinsTCA , LRG_530:g.31677_31679delinsTCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000556892.6:c.*643_*645delinsTCA	ENSP00000452206.2:n.*643_*645delinsTCA
ENST00000556979.6:c.*1579_*1581delinsTCA	ENSP00000452378.1:n.*1579_*1581delinsTCA
ENST00000358664.9:c.*643_*645delinsTCA MANE Select	ENSP00000351490.4:n.*643_*645delinsTCA
ENST00000651648.1:c.145-5464_145-5462delinsTCA	ENSP00000498863.1:n.145-5464_145-5462delinsTCA
ENST00000284165.10:c.*1970_*1972delinsTCA	ENSP00000284165.6:n.*1970_*1972delinsTCA
ENST00000341653.6:c.171+17875_171+17877delinsTCA	ENSP00000342482.2:n.171+17875_171+17877delinsTCA
ENST00000358402.8:c.*643_*645delinsTCA	ENSP00000351175.4:n.*643_*645delinsTCA
ENST00000358664.8:c.*643_*645delinsTCA	ENSP00000351490.4:n.*643_*645delinsTCA
ENST00000394606.6:c.*899_*901delinsTCA	ENSP00000378104.2:n.*899_*901delinsTCA
ENST00000555932.5:c.*618_*620delinsTCA	ENSP00000450763.1:n.*618_*620delinsTCA
ENST00000618858.4:c.*915_*917delinsTCA	ENSP00000480127.1:n.*915_*917delinsTCA
NM_001271069.1:c.144+17875_144+17877delinsTCA	NP_001257998.1:n.144+17875_144+17877delinsTCA
NM_002382.4:c.*643_*645delinsTCA	NP_002373.3:n.*643_*645delinsTCA
NM_145112.2:c.*643_*645delinsTCA	NP_660087.1:n.*643_*645delinsTCA
NM_145113.2:c.*915_*917delinsTCA	NP_660088.1:n.*915_*917delinsTCA
NM_197957.3:c.171+17875_171+17877delinsTCA	NP_932061.1:n.171+17875_171+17877delinsTCA
NR_073137.1:n.1250_1252delinsTCA
XR_429315.2:n.1413_1415delinsTCA
NM_001320415.1:c.*643_*645delinsTCA	NP_001307344.1:n.*643_*645delinsTCA
XM_017021312.2:c.*643_*645delinsTCA	XP_016876801.1:n.*643_*645delinsTCA
XM_017021313.1:c.*643_*645delinsTCA	XP_016876802.1:n.*643_*645delinsTCA
XR_001750326.2:n.1471_1473delinsTCA
XR_001750327.2:n.1390_1392delinsTCA
XR_002957553.1:n.1904_1906delinsTCA
XR_943450.3:n.1494_1496delinsTCA
XR_943451.3:n.1510_1512delinsTCA
XR_943452.3:n.1455_1457delinsTCA
NM_001320415.2:c.*643_*645delinsTCA	NP_001307344.1:n.*643_*645delinsTCA
NM_002382.5:c.*643_*645delinsTCA MANE Select	NP_002373.3:n.*643_*645delinsTCA
NM_145112.3:c.*643_*645delinsTCA	NP_660087.1:n.*643_*645delinsTCA
NM_145113.3:c.*915_*917delinsTCA	NP_660088.1:n.*915_*917delinsTCA
NM_001271069.2:c.144+17875_144+17877delinsTCA	NP_001257998.1:n.144+17875_144+17877delinsTCA
NM_197957.4:c.171+17875_171+17877delinsTCA	NP_932061.1:n.171+17875_171+17877delinsTCA