Canonical Allele Identifier: CA1480066746

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583482_99583483delinsCA , CM000666.2:g.99583482_99583483delinsCA	GRCh38
NC_000004.11:g.100504639_100504640delinsCA , CM000666.1:g.100504639_100504640delinsCA	GRCh37
NC_000004.10:g.100723662_100723663delinsCA	NCBI36
NG_011469.1:g.24400_24401delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.358_359delinsCA MANE Select	ENSP00000265517.5:p.Gln120=
ENST00000457717.6:c.358_359delinsCA	ENSP00000400821.1:p.Gln120=
ENST00000511045.6:c.109_110delinsCA	ENSP00000427679.2:p.Gln37=
ENST00000265517.9:c.358_359delinsCA	ENSP00000265517.5:p.Gln120=
ENST00000422897.6:c.358_359delinsCA	ENSP00000407350.2:p.Gln120=
ENST00000457717.5:c.358_359delinsCA	ENSP00000400821.1:p.Gln120=
ENST00000506883.5:c.388_389delinsCA	ENSP00000426755.1:p.Gln130=
ENST00000511045.5:c.439_440delinsCA	ENSP00000427679.1:p.Gln147=
ENST00000619629.1:c.358_359delinsCA	ENSP00000482850.1:p.Gln120=
NM_000253.3:c.358_359delinsCA	NP_000244.2:p.Gln120=
NM_001300785.1:c.439_440delinsCA	NP_001287714.1:p.Gln147=
NM_000253.4:c.358_359delinsCA	NP_000244.2:p.Gln120=
NM_001300785.2:c.109_110delinsCA	NP_001287714.2:p.Gln37=
NM_001386140.1:c.358_359delinsCA MANE Select	NP_001373069.1:p.Gln120=