Canonical Allele Identifier: CA2625289375

Gene: MAX

Linked Data

• gnomAD v4: 14-65075960-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075960_65075961insT , CM000676.2:g.65075960_65075961insT	GRCh38
NC_000014.8:g.65542678_65542679insT , CM000676.1:g.65542678_65542679insT	GRCh37
NC_000014.7:g.64612431_64612432insT	NCBI36
NG_029830.1:g.31549_31550insA , LRG_530:g.31549_31550insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*515_*516insA	ENSP00000452206.2:n.*515_*516insA
ENST00000556979.6:c.*1451_*1452insA	ENSP00000452378.1:n.*1451_*1452insA
ENST00000358664.9:c.*515_*516insA MANE Select	ENSP00000351490.4:n.*515_*516insA
ENST00000651648.1:c.145-5592_145-5591insA	ENSP00000498863.1:n.145-5592_145-5591insA
ENST00000284165.10:c.*1842_*1843insA	ENSP00000284165.6:n.*1842_*1843insA
ENST00000341653.6:c.171+17747_171+17748insA	ENSP00000342482.2:n.171+17747_171+17748insA
ENST00000358402.8:c.*515_*516insA	ENSP00000351175.4:n.*515_*516insA
ENST00000358664.8:c.*515_*516insA	ENSP00000351490.4:n.*515_*516insA
ENST00000394606.6:c.*771_*772insA	ENSP00000378104.2:n.*771_*772insA
ENST00000555932.5:c.*490_*491insA	ENSP00000450763.1:n.*490_*491insA
ENST00000618858.4:c.*787_*788insA	ENSP00000480127.1:n.*787_*788insA
NM_001271069.1:c.144+17747_144+17748insA	NP_001257998.1:n.144+17747_144+17748insA
NM_002382.4:c.*515_*516insA	NP_002373.3:n.*515_*516insA
NM_145112.2:c.*515_*516insA	NP_660087.1:n.*515_*516insA
NM_145113.2:c.*787_*788insA	NP_660088.1:n.*787_*788insA
NM_197957.3:c.171+17747_171+17748insA	NP_932061.1:n.171+17747_171+17748insA
NR_073137.1:n.1122_1123insA
XR_429315.2:n.1285_1286insA
NM_001320415.1:c.*515_*516insA	NP_001307344.1:n.*515_*516insA
XM_017021312.2:c.*515_*516insA	XP_016876801.1:n.*515_*516insA
XM_017021313.1:c.*515_*516insA	XP_016876802.1:n.*515_*516insA
XR_001750326.2:n.1343_1344insA
XR_001750327.2:n.1262_1263insA
XR_002957553.1:n.1776_1777insA
XR_943450.3:n.1366_1367insA
XR_943451.3:n.1382_1383insA
XR_943452.3:n.1327_1328insA
NM_001320415.2:c.*515_*516insA	NP_001307344.1:n.*515_*516insA
NM_002382.5:c.*515_*516insA MANE Select	NP_002373.3:n.*515_*516insA
NM_145112.3:c.*515_*516insA	NP_660087.1:n.*515_*516insA
NM_145113.3:c.*787_*788insA	NP_660088.1:n.*787_*788insA
NM_001271069.2:c.144+17747_144+17748insA	NP_001257998.1:n.144+17747_144+17748insA
NM_197957.4:c.171+17747_171+17748insA	NP_932061.1:n.171+17747_171+17748insA