Canonical Allele Identifier: CA262716179

Gene: MAX

Linked Data

• dbSNP Id: rs946883932
• gnomAD v3: 14-65075154-T-C
• gnomAD v4: 14-65075154-T-C
• MyVariant Identifiers: chr14:g.65541872T>C (hg19) ; chr14:g.65075154T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075154T>C , CM000676.2:g.65075154T>C	GRCh38
NC_000014.8:g.65541872T>C , CM000676.1:g.65541872T>C	GRCh37
NC_000014.7:g.64611625T>C	NCBI36
NG_029830.1:g.32356A>G , LRG_530:g.32356A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*2258A>G	ENSP00000452378.1:n.*2258A>G
ENST00000358664.9:c.*1322A>G MANE Select	ENSP00000351490.4:n.*1322A>G
ENST00000651648.1:c.145-4785A>G	ENSP00000498863.1:n.145-4785A>G
ENST00000341653.6:c.171+18554A>G	ENSP00000342482.2:n.171+18554A>G
ENST00000358402.8:c.*1322A>G	ENSP00000351175.4:n.*1322A>G
ENST00000394606.6:c.*1578A>G	ENSP00000378104.2:n.*1578A>G
ENST00000618858.4:c.*1594A>G	ENSP00000480127.1:n.*1594A>G
NM_001271069.1:c.144+18554A>G	NP_001257998.1:n.144+18554A>G
NM_002382.4:c.*1322A>G	NP_002373.3:n.*1322A>G
NM_145112.2:c.*1322A>G	NP_660087.1:n.*1322A>G
NM_145113.2:c.*1594A>G	NP_660088.1:n.*1594A>G
NM_197957.3:c.171+18554A>G	NP_932061.1:n.171+18554A>G
NR_073137.1:n.1929A>G
XR_429315.2:n.2092A>G
NM_001320415.1:c.*1322A>G	NP_001307344.1:n.*1322A>G
XM_017021312.2:c.*1322A>G	XP_016876801.1:n.*1322A>G
XM_017021313.1:c.*1322A>G	XP_016876802.1:n.*1322A>G
XR_001750326.2:n.2150A>G
XR_001750327.2:n.2069A>G
XR_002957553.1:n.2583A>G
XR_943450.3:n.2173A>G
XR_943451.3:n.2189A>G
XR_943452.3:n.2134A>G
NM_001320415.2:c.*1322A>G	NP_001307344.1:n.*1322A>G
NM_002382.5:c.*1322A>G MANE Select	NP_002373.3:n.*1322A>G
NM_145112.3:c.*1322A>G	NP_660087.1:n.*1322A>G
NM_145113.3:c.*1594A>G	NP_660088.1:n.*1594A>G
NM_001271069.2:c.144+18554A>G	NP_001257998.1:n.144+18554A>G
NM_197957.4:c.171+18554A>G	NP_932061.1:n.171+18554A>G