Canonical Allele Identifier: CA2625289017

Gene: MAX

Linked Data

• gnomAD v4: 14-65075551-T-TCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075553_65075554insGCA , CM000676.2:g.65075553_65075554insGCA	GRCh38
NC_000014.8:g.65542271_65542272insGCA , CM000676.1:g.65542271_65542272insGCA	GRCh37
NC_000014.7:g.64612024_64612025insGCA	NCBI36
NG_029830.1:g.31958_31959insCTG , LRG_530:g.31958_31959insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*924_*925insCTG	ENSP00000452206.2:n.*924_*925insCTG
ENST00000556979.6:c.*1860_*1861insCTG	ENSP00000452378.1:n.*1860_*1861insCTG
ENST00000358664.9:c.*924_*925insCTG MANE Select	ENSP00000351490.4:n.*924_*925insCTG
ENST00000651648.1:c.145-5183_145-5182insCTG	ENSP00000498863.1:n.145-5183_145-5182insCTG
ENST00000284165.10:c.*2251_*2252insCTG	ENSP00000284165.6:n.*2251_*2252insCTG
ENST00000341653.6:c.171+18156_171+18157insCTG	ENSP00000342482.2:n.171+18156_171+18157insCTG
ENST00000358402.8:c.*924_*925insCTG	ENSP00000351175.4:n.*924_*925insCTG
ENST00000358664.8:c.*924_*925insCTG	ENSP00000351490.4:n.*924_*925insCTG
ENST00000394606.6:c.*1180_*1181insCTG	ENSP00000378104.2:n.*1180_*1181insCTG
ENST00000555932.5:c.*899_*900insCTG	ENSP00000450763.1:n.*899_*900insCTG
ENST00000618858.4:c.*1196_*1197insCTG	ENSP00000480127.1:n.*1196_*1197insCTG
NM_001271069.1:c.144+18156_144+18157insCTG	NP_001257998.1:n.144+18156_144+18157insCTG
NM_002382.4:c.*924_*925insCTG	NP_002373.3:n.*924_*925insCTG
NM_145112.2:c.*924_*925insCTG	NP_660087.1:n.*924_*925insCTG
NM_145113.2:c.*1196_*1197insCTG	NP_660088.1:n.*1196_*1197insCTG
NM_197957.3:c.171+18156_171+18157insCTG	NP_932061.1:n.171+18156_171+18157insCTG
NR_073137.1:n.1531_1532insCTG
XR_429315.2:n.1694_1695insCTG
NM_001320415.1:c.*924_*925insCTG	NP_001307344.1:n.*924_*925insCTG
XM_017021312.2:c.*924_*925insCTG	XP_016876801.1:n.*924_*925insCTG
XM_017021313.1:c.*924_*925insCTG	XP_016876802.1:n.*924_*925insCTG
XR_001750326.2:n.1752_1753insCTG
XR_001750327.2:n.1671_1672insCTG
XR_002957553.1:n.2185_2186insCTG
XR_943450.3:n.1775_1776insCTG
XR_943451.3:n.1791_1792insCTG
XR_943452.3:n.1736_1737insCTG
NM_001320415.2:c.*924_*925insCTG	NP_001307344.1:n.*924_*925insCTG
NM_002382.5:c.*924_*925insCTG MANE Select	NP_002373.3:n.*924_*925insCTG
NM_145112.3:c.*924_*925insCTG	NP_660087.1:n.*924_*925insCTG
NM_145113.3:c.*1196_*1197insCTG	NP_660088.1:n.*1196_*1197insCTG
NM_001271069.2:c.144+18156_144+18157insCTG	NP_001257998.1:n.144+18156_144+18157insCTG
NM_197957.4:c.171+18156_171+18157insCTG	NP_932061.1:n.171+18156_171+18157insCTG