Canonical Allele Identifier: CA2142951448

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076157_65076159delinsCTA , CM000676.2:g.65076157_65076159delinsCTA	GRCh38
NC_000014.8:g.65542875_65542877delinsCTA , CM000676.1:g.65542875_65542877delinsCTA	GRCh37
NC_000014.7:g.64612628_64612630delinsCTA	NCBI36
NG_029830.1:g.31351_31353delinsTAG , LRG_530:g.31351_31353delinsTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*317_*319delinsTAG	ENSP00000452206.2:n.*317_*319delinsTAG
ENST00000556979.6:c.*1253_*1255delinsTAG	ENSP00000452378.1:n.*1253_*1255delinsTAG
ENST00000358664.9:c.*317_*319delinsTAG MANE Select	ENSP00000351490.4:n.*317_*319delinsTAG
ENST00000651648.1:c.145-5790_145-5788delinsTAG	ENSP00000498863.1:n.145-5790_145-5788delinsTAG
ENST00000284165.10:c.*1644_*1646delinsTAG	ENSP00000284165.6:n.*1644_*1646delinsTAG
ENST00000341653.6:c.171+17549_171+17551delinsTAG	ENSP00000342482.2:n.171+17549_171+17551delinsTAG
ENST00000358402.8:c.*317_*319delinsTAG	ENSP00000351175.4:n.*317_*319delinsTAG
ENST00000358664.8:c.*317_*319delinsTAG	ENSP00000351490.4:n.*317_*319delinsTAG
ENST00000394606.6:c.*573_*575delinsTAG	ENSP00000378104.2:n.*573_*575delinsTAG
ENST00000555419.5:c.692_694delinsTAG	ENSP00000452405.1:n.692_694delinsTAG
ENST00000555932.5:c.*292_*294delinsTAG	ENSP00000450763.1:n.*292_*294delinsTAG
ENST00000618858.4:c.*589_*591delinsTAG	ENSP00000480127.1:n.*589_*591delinsTAG
NM_001271069.1:c.144+17549_144+17551delinsTAG	NP_001257998.1:n.144+17549_144+17551delinsTAG
NM_002382.4:c.*317_*319delinsTAG	NP_002373.3:n.*317_*319delinsTAG
NM_145112.2:c.*317_*319delinsTAG	NP_660087.1:n.*317_*319delinsTAG
NM_145113.2:c.*589_*591delinsTAG	NP_660088.1:n.*589_*591delinsTAG
NM_197957.3:c.171+17549_171+17551delinsTAG	NP_932061.1:n.171+17549_171+17551delinsTAG
NR_073137.1:n.924_926delinsTAG
XR_429315.2:n.1087_1089delinsTAG
NM_001320415.1:c.*317_*319delinsTAG	NP_001307344.1:n.*317_*319delinsTAG
XM_017021312.2:c.*317_*319delinsTAG	XP_016876801.1:n.*317_*319delinsTAG
XM_017021313.1:c.*317_*319delinsTAG	XP_016876802.1:n.*317_*319delinsTAG
XR_001750326.2:n.1145_1147delinsTAG
XR_001750327.2:n.1064_1066delinsTAG
XR_002957553.1:n.1578_1580delinsTAG
XR_943450.3:n.1168_1170delinsTAG
XR_943451.3:n.1184_1186delinsTAG
XR_943452.3:n.1129_1131delinsTAG
NM_001320415.2:c.*317_*319delinsTAG	NP_001307344.1:n.*317_*319delinsTAG
NM_002382.5:c.*317_*319delinsTAG MANE Select	NP_002373.3:n.*317_*319delinsTAG
NM_145112.3:c.*317_*319delinsTAG	NP_660087.1:n.*317_*319delinsTAG
NM_145113.3:c.*589_*591delinsTAG	NP_660088.1:n.*589_*591delinsTAG
NM_001271069.2:c.144+17549_144+17551delinsTAG	NP_001257998.1:n.144+17549_144+17551delinsTAG
NM_197957.4:c.171+17549_171+17551delinsTAG	NP_932061.1:n.171+17549_171+17551delinsTAG