Canonical Allele Identifier: CA390031417

Gene: MAX

Linked Data

• MyVariant Identifiers: chr14:g.65543254G>C (hg19) ; chr14:g.65076536G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076536G>C , CM000676.2:g.65076536G>C	GRCh38
NC_000014.8:g.65543254G>C , CM000676.1:g.65543254G>C	GRCh37
NC_000014.7:g.64613007G>C	NCBI36
NG_029830.1:g.30974C>G , LRG_530:g.30974C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.204C>G	ENSP00000452206.2:p.Ser68Arg
ENST00000556979.6:c.*876C>G	ENSP00000452378.1:n.*876C>G
ENST00000358664.9:c.423C>G MANE Select	ENSP00000351490.4:p.Ser141Arg
ENST00000651648.1:c.145-6167C>G	ENSP00000498863.1:n.145-6167C>G
ENST00000284165.10:c.*1267C>G	ENSP00000284165.6:n.*1267C>G
ENST00000341653.6:c.171+17172C>G	ENSP00000342482.2:n.171+17172C>G
ENST00000358402.8:c.396C>G	ENSP00000351175.4:p.Ser132Arg
ENST00000358664.8:c.423C>G	ENSP00000351490.4:p.Ser141Arg
ENST00000394606.6:c.*196C>G	ENSP00000378104.2:n.*196C>G
ENST00000553928.5:c.*212C>G	ENSP00000451907.1:n.*212C>G
ENST00000555419.5:c.315C>G	ENSP00000452405.1:p.Ser105Arg
ENST00000555932.5:c.164C>G	ENSP00000450763.1:p.Ala55Gly
ENST00000557277.5:c.234C>G	ENSP00000450955.1:p.Ser78Arg
ENST00000618858.4:c.*212C>G	ENSP00000480127.1:n.*212C>G
NM_001271069.1:c.144+17172C>G	NP_001257998.1:n.144+17172C>G
NM_002382.4:c.423C>G	NP_002373.3:p.Ser141Arg
NM_145112.2:c.396C>G	NP_660087.1:p.Ser132Arg
NM_145113.2:c.*212C>G	NP_660088.1:n.*212C>G
NM_197957.3:c.171+17172C>G	NP_932061.1:n.171+17172C>G
NR_073137.1:n.547C>G
XR_429315.2:n.710C>G
NM_001320415.1:c.234C>G	NP_001307344.1:p.Ser78Arg
XM_017021312.2:c.234C>G	XP_016876801.1:p.Ser78Arg
XM_017021313.1:c.234C>G	XP_016876802.1:p.Ser78Arg
XR_001750326.2:n.768C>G
XR_001750327.2:n.687C>G
XR_002957553.1:n.1201C>G
XR_943450.3:n.791C>G
XR_943451.3:n.807C>G
XR_943452.3:n.752C>G
NM_001320415.2:c.234C>G	NP_001307344.1:p.Ser78Arg
NM_002382.5:c.423C>G MANE Select	NP_002373.3:p.Ser141Arg
NM_145112.3:c.396C>G	NP_660087.1:p.Ser132Arg
NM_145113.3:c.*212C>G	NP_660088.1:n.*212C>G
NM_001271069.2:c.144+17172C>G	NP_001257998.1:n.144+17172C>G
NM_197957.4:c.171+17172C>G	NP_932061.1:n.171+17172C>G