Canonical Allele Identifier: CA1480079187

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99600691_99600692delinsAT , CM000666.2:g.99600691_99600692delinsAT	GRCh38
NC_000004.11:g.100521848_100521849delinsAT , CM000666.1:g.100521848_100521849delinsAT	GRCh37
NC_000004.10:g.100740871_100740872delinsAT	NCBI36
NG_011469.1:g.41609_41610delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.1194_1195delinsAT MANE Select	ENSP00000265517.5:p.Gly398=
ENST00000457717.6:c.1194_1195delinsAT	ENSP00000400821.1:p.Gly398=
ENST00000511045.6:c.945_946delinsAT	ENSP00000427679.2:p.Gly315=
ENST00000265517.9:c.1194_1195delinsAT	ENSP00000265517.5:p.Gly398=
ENST00000457717.5:c.1194_1195delinsAT	ENSP00000400821.1:p.Gly398=
ENST00000511045.5:c.1275_1276delinsAT	ENSP00000427679.1:p.Gly425=
ENST00000619629.1:c.1194_1195delinsAT	ENSP00000482850.1:p.Gly398=
NM_000253.3:c.1194_1195delinsAT	NP_000244.2:p.Gly398=
NM_001300785.1:c.1275_1276delinsAT	NP_001287714.1:p.Gly425=
NM_000253.4:c.1194_1195delinsAT	NP_000244.2:p.Gly398=
NM_001300785.2:c.945_946delinsAT	NP_001287714.2:p.Gly315=
NM_001386140.1:c.1194_1195delinsAT MANE Select	NP_001373069.1:p.Gly398=