Canonical Allele Identifier: CA707784013

Gene: MAX

Linked Data

• dbSNP Id: rs1356464094
• gnomAD v2: 14-65541841-CAAG-C
• gnomAD v3: 14-65075123-CAAG-C
• gnomAD v4: 14-65075123-CAAG-C
• MyVariant Identifiers: chr14:g.65541842_65541844del (hg19) ; chr14:g.65075124_65075126del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075127_65075129del , CM000676.2:g.65075127_65075129del	GRCh38
NC_000014.8:g.65541845_65541847del , CM000676.1:g.65541845_65541847del	GRCh37
NC_000014.7:g.64611598_64611600del	NCBI36
NG_029830.1:g.32384_32386del , LRG_530:g.32384_32386del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651648.1:c.145-4757_145-4755del	ENSP00000498863.1:n.145-4757_145-4755del
ENST00000341653.6:c.171+18582_171+18584del	ENSP00000342482.2:n.171+18582_171+18584del
ENST00000358402.8:c.*1350_*1352del	ENSP00000351175.4:n.*1350_*1352del
ENST00000618858.4:c.*1622_*1624del	ENSP00000480127.1:n.*1622_*1624del
NM_001271069.1:c.144+18582_144+18584del	NP_001257998.1:n.144+18582_144+18584del
NM_002382.4:c.*1350_*1352del	NP_002373.3:n.*1350_*1352del
NM_145112.2:c.*1350_*1352del	NP_660087.1:n.*1350_*1352del
NM_145113.2:c.*1622_*1624del	NP_660088.1:n.*1622_*1624del
NM_197957.3:c.171+18582_171+18584del	NP_932061.1:n.171+18582_171+18584del
NR_073137.1:n.1957_1959del
NM_001320415.1:c.*1350_*1352del	NP_001307344.1:n.*1350_*1352del
NM_001271069.2:c.144+18582_144+18584del	NP_001257998.1:n.144+18582_144+18584del
NM_197957.4:c.171+18582_171+18584del	NP_932061.1:n.171+18582_171+18584del