Canonical Allele Identifier: CA1480066535
Gene: MTTP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99583384_99583385delinsTA , CM000666.2:g.99583384_99583385delinsTA GRCh38
NC_000004.11:g.100504541_100504542delinsTA , CM000666.1:g.100504541_100504542delinsTA GRCh37
NC_000004.10:g.100723564_100723565delinsTA NCBI36
NG_011469.1:g.24302_24303delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000265517.10:c.260_261delinsTA MANE Select ENSP00000265517.5:p.Val87=
ENST00000457717.6:c.260_261delinsTA ENSP00000400821.1:p.Val87=
ENST00000505094.6:c.11_12delinsTA ENSP00000422782.2:p.Val4=
ENST00000511045.6:c.11_12delinsTA ENSP00000427679.2:p.Val4=
ENST00000265517.9:c.260_261delinsTA ENSP00000265517.5:p.Val87=
ENST00000422897.6:c.260_261delinsTA ENSP00000407350.2:p.Val87=
ENST00000457717.5:c.260_261delinsTA ENSP00000400821.1:p.Val87=
ENST00000505094.5:c.*350_*351delinsTA ENSP00000422782.1:n.*350_*351delinsTA
ENST00000506883.5:c.290_291delinsTA ENSP00000426755.1:p.Val97=
ENST00000511045.5:c.341_342delinsTA ENSP00000427679.1:p.Val114=
ENST00000513404.5:c.*323_*324delinsTA ENSP00000424972.1:n.*323_*324delinsTA
ENST00000515141.5:c.*323_*324delinsTA ENSP00000425642.1:n.*323_*324delinsTA
ENST00000619629.1:c.260_261delinsTA ENSP00000482850.1:p.Val87=
NM_000253.3:c.260_261delinsTA NP_000244.2:p.Val87=
NM_001300785.1:c.341_342delinsTA NP_001287714.1:p.Val114=
NM_000253.4:c.260_261delinsTA NP_000244.2:p.Val87=
NM_001300785.2:c.11_12delinsTA NP_001287714.2:p.Val4=
NM_001386140.1:c.260_261delinsTA MANE Select NP_001373069.1:p.Val87=