Canonical Allele Identifier: CA964079299

Gene: MAX

Linked Data

• gnomAD v3: 14-65075124-A-G
• gnomAD v4: 14-65075124-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075124A>G , CM000676.2:g.65075124A>G	GRCh38
NC_000014.8:g.65541842A>G , CM000676.1:g.65541842A>G	GRCh37
NC_000014.7:g.64611595A>G	NCBI36
NG_029830.1:g.32386T>C , LRG_530:g.32386T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651648.1:c.145-4755T>C	ENSP00000498863.1:n.145-4755T>C
ENST00000341653.6:c.171+18584T>C	ENSP00000342482.2:n.171+18584T>C
ENST00000358402.8:c.*1352T>C	ENSP00000351175.4:n.*1352T>C
ENST00000618858.4:c.*1624T>C	ENSP00000480127.1:n.*1624T>C
NM_001271069.1:c.144+18584T>C	NP_001257998.1:n.144+18584T>C
NM_002382.4:c.*1352T>C	NP_002373.3:n.*1352T>C
NM_145112.2:c.*1352T>C	NP_660087.1:n.*1352T>C
NM_145113.2:c.*1624T>C	NP_660088.1:n.*1624T>C
NM_197957.3:c.171+18584T>C	NP_932061.1:n.171+18584T>C
NR_073137.1:n.1959T>C
NM_001320415.1:c.*1352T>C	NP_001307344.1:n.*1352T>C
NM_001271069.2:c.144+18584T>C	NP_001257998.1:n.144+18584T>C
NM_197957.4:c.171+18584T>C	NP_932061.1:n.171+18584T>C