Canonical Allele Identifier: CA2762812236

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99600855_99600856insC , CM000666.2:g.99600855_99600856insC	GRCh38
NC_000004.11:g.100522012_100522013insC , CM000666.1:g.100522012_100522013insC	GRCh37
NC_000004.10:g.100741035_100741036insC	NCBI36
NG_011469.1:g.41773_41774insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.1236+122_1236+123insC MANE Select	ENSP00000265517.5:n.1236+122_1236+123insC
ENST00000457717.6:c.1236+122_1236+123insC	ENSP00000400821.1:n.1236+122_1236+123insC
ENST00000511045.6:c.987+122_987+123insC	ENSP00000427679.2:n.987+122_987+123insC
ENST00000265517.9:c.1236+122_1236+123insC	ENSP00000265517.5:n.1236+122_1236+123insC
ENST00000457717.5:c.1236+122_1236+123insC	ENSP00000400821.1:n.1236+122_1236+123insC
ENST00000511045.5:c.1317+122_1317+123insC	ENSP00000427679.1:n.1317+122_1317+123insC
ENST00000619629.1:c.1236+122_1236+123insC	ENSP00000482850.1:n.1236+122_1236+123insC
NM_000253.3:c.1236+122_1236+123insC	NP_000244.2:n.1236+122_1236+123insC
NM_001300785.1:c.1317+122_1317+123insC	NP_001287714.1:n.1317+122_1317+123insC
NM_000253.4:c.1236+122_1236+123insC	NP_000244.2:n.1236+122_1236+123insC
NM_001300785.2:c.987+122_987+123insC	NP_001287714.2:n.987+122_987+123insC
NM_001386140.1:c.1236+122_1236+123insC MANE Select	NP_001373069.1:n.1236+122_1236+123insC