Canonical Allele Identifier: CA2762812166

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99600782_99600783insAGG , CM000666.2:g.99600782_99600783insAGG	GRCh38
NC_000004.11:g.100521939_100521940insAGG , CM000666.1:g.100521939_100521940insAGG	GRCh37
NC_000004.10:g.100740962_100740963insAGG	NCBI36
NG_011469.1:g.41700_41701insAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.1236+49_1236+50insAGG MANE Select	ENSP00000265517.5:n.1236+49_1236+50insAGG
ENST00000457717.6:c.1236+49_1236+50insAGG	ENSP00000400821.1:n.1236+49_1236+50insAGG
ENST00000511045.6:c.987+49_987+50insAGG	ENSP00000427679.2:n.987+49_987+50insAGG
ENST00000265517.9:c.1236+49_1236+50insAGG	ENSP00000265517.5:n.1236+49_1236+50insAGG
ENST00000457717.5:c.1236+49_1236+50insAGG	ENSP00000400821.1:n.1236+49_1236+50insAGG
ENST00000511045.5:c.1317+49_1317+50insAGG	ENSP00000427679.1:n.1317+49_1317+50insAGG
ENST00000619629.1:c.1236+49_1236+50insAGG	ENSP00000482850.1:n.1236+49_1236+50insAGG
NM_000253.3:c.1236+49_1236+50insAGG	NP_000244.2:n.1236+49_1236+50insAGG
NM_001300785.1:c.1317+49_1317+50insAGG	NP_001287714.1:n.1317+49_1317+50insAGG
NM_000253.4:c.1236+49_1236+50insAGG	NP_000244.2:n.1236+49_1236+50insAGG
NM_001300785.2:c.987+49_987+50insAGG	NP_001287714.2:n.987+49_987+50insAGG
NM_001386140.1:c.1236+49_1236+50insAGG MANE Select	NP_001373069.1:n.1236+49_1236+50insAGG