Canonical Allele Identifier: CA2625290781

Gene: MAX

Linked Data

• gnomAD v4: 14-65078187-CTTTATTTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65078199_65078206del , CM000676.2:g.65078199_65078206del	GRCh38
NC_000014.8:g.65544917_65544924del , CM000676.1:g.65544917_65544924del	GRCh37
NC_000014.7:g.64614670_64614677del	NCBI36
NG_029830.1:g.29315_29322del , LRG_530:g.29315_29322del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.-48-159_-48-152del	ENSP00000452206.2:n.-48-159_-48-152del
ENST00000556979.6:c.172-159_172-152del	ENSP00000452378.1:n.172-159_172-152del
ENST00000358664.9:c.172-159_172-152del MANE Select	ENSP00000351490.4:n.172-159_172-152del
ENST00000651648.1:c.145-7826_145-7819del	ENSP00000498863.1:n.145-7826_145-7819del
ENST00000284165.10:c.172-159_172-152del	ENSP00000284165.6:n.172-159_172-152del
ENST00000341653.6:c.171+15513_171+15520del	ENSP00000342482.2:n.171+15513_171+15520del
ENST00000358402.8:c.145-159_145-152del	ENSP00000351175.4:n.145-159_145-152del
ENST00000358664.8:c.172-159_172-152del	ENSP00000351490.4:n.172-159_172-152del
ENST00000394606.6:c.172-159_172-152del	ENSP00000378104.2:n.172-159_172-152del
ENST00000553928.5:c.172-159_172-152del	ENSP00000451907.1:n.172-159_172-152del
ENST00000553951.1:n.249-159_249-152del
ENST00000555419.5:c.64-159_64-152del	ENSP00000452405.1:n.64-159_64-152del
ENST00000555667.5:c.145-159_145-152del	ENSP00000452286.1:n.145-159_145-152del
ENST00000555932.5:c.37-1532_37-1525del	ENSP00000450763.1:n.37-1532_37-1525del
ENST00000556443.5:c.145-159_145-152del	ENSP00000450818.1:n.145-159_145-152del
ENST00000556892.5:c.-48-159_-48-152del	ENSP00000452206.1:n.-48-159_-48-152del
ENST00000556979.5:c.172-159_172-152del	ENSP00000452378.1:n.172-159_172-152del
ENST00000557277.5:c.-103-159_-103-152del	ENSP00000450955.1:n.-103-159_-103-152del
ENST00000557746.5:c.145-159_145-152del	ENSP00000452197.1:n.145-159_145-152del
ENST00000618858.4:c.172-159_172-152del	ENSP00000480127.1:n.172-159_172-152del
NM_001271069.1:c.144+15513_144+15520del	NP_001257998.1:n.144+15513_144+15520del
NM_002382.4:c.172-159_172-152del	NP_002373.3:n.172-159_172-152del
NM_145112.2:c.145-159_145-152del	NP_660087.1:n.145-159_145-152del
NM_145113.2:c.172-159_172-152del	NP_660088.1:n.172-159_172-152del
NM_197957.3:c.171+15513_171+15520del	NP_932061.1:n.171+15513_171+15520del
NR_073137.1:n.296-159_296-152del
XM_011536773.1:c.172-159_172-152del	XP_011535075.1:n.172-159_172-152del
XR_429315.2:n.374-159_374-152del
XR_943450.1:n.374-159_374-152del
XR_943451.1:n.374-159_374-152del
XR_943452.1:n.336-159_336-152del
NM_001320415.1:c.-103-159_-103-152del	NP_001307344.1:n.-103-159_-103-152del
XM_011536773.3:c.172-159_172-152del	XP_011535075.1:n.172-159_172-152del
XM_017021312.2:c.-103-159_-103-152del	XP_016876801.1:n.-103-159_-103-152del
XM_017021313.1:c.-103-159_-103-152del	XP_016876802.1:n.-103-159_-103-152del
XR_001750326.2:n.335-159_335-152del
XR_001750327.2:n.335-159_335-152del
XR_002957553.1:n.365-159_365-152del
XR_943450.3:n.374-159_374-152del
XR_943451.3:n.374-159_374-152del
XR_943452.3:n.335-159_335-152del
NM_001320415.2:c.-103-159_-103-152del	NP_001307344.1:n.-103-159_-103-152del
NM_002382.5:c.172-159_172-152del MANE Select	NP_002373.3:n.172-159_172-152del
NM_145112.3:c.145-159_145-152del	NP_660087.1:n.145-159_145-152del
NM_145113.3:c.172-159_172-152del	NP_660088.1:n.172-159_172-152del
NM_001271069.2:c.144+15513_144+15520del	NP_001257998.1:n.144+15513_144+15520del
NM_197957.4:c.171+15513_171+15520del	NP_932061.1:n.171+15513_171+15520del