Canonical Allele Identifier: CA1480088028

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622889_99622891delinsAGG , CM000666.2:g.99622889_99622891delinsAGG	GRCh38
NC_000004.11:g.100544046_100544048delinsAGG , CM000666.1:g.100544046_100544048delinsAGG	GRCh37
NC_000004.10:g.100763069_100763071delinsAGG	NCBI36
NG_011469.1:g.63807_63809delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.*41_*43delinsAGG MANE Select	ENSP00000265517.5:n.*41_*43delinsAGG
ENST00000457717.6:c.*41_*43delinsAGG	ENSP00000400821.1:n.*41_*43delinsAGG
ENST00000511045.6:c.*41_*43delinsAGG	ENSP00000427679.2:n.*41_*43delinsAGG
ENST00000265517.9:c.*41_*43delinsAGG	ENSP00000265517.5:n.*41_*43delinsAGG
ENST00000457717.5:c.*41_*43delinsAGG	ENSP00000400821.1:n.*41_*43delinsAGG
ENST00000511045.5:c.*41_*43delinsAGG	ENSP00000427679.1:n.*41_*43delinsAGG
ENST00000619629.1:c.*1173_*1175delinsAGG	ENSP00000482850.1:n.*1173_*1175delinsAGG
NM_000253.3:c.*41_*43delinsAGG	NP_000244.2:n.*41_*43delinsAGG
NM_001300785.1:c.*41_*43delinsAGG	NP_001287714.1:n.*41_*43delinsAGG
NM_000253.4:c.*41_*43delinsAGG	NP_000244.2:n.*41_*43delinsAGG
NM_001300785.2:c.*41_*43delinsAGG	NP_001287714.2:n.*41_*43delinsAGG
NM_001386140.1:c.*41_*43delinsAGG MANE Select	NP_001373069.1:n.*41_*43delinsAGG