Canonical Allele Identifier: CA102631742

Gene: MTTP

Linked Data

• dbSNP Id: rs34350284
• MyVariant Identifiers: chr4:g.100522014_100522015insG (hg19) ; chr4:g.99600857_99600858insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99600857_99600858insG , CM000666.2:g.99600857_99600858insG	GRCh38
NC_000004.11:g.100522014_100522015insG , CM000666.1:g.100522014_100522015insG	GRCh37
NC_000004.10:g.100741037_100741038insG	NCBI36
NG_011469.1:g.41775_41776insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.1236+124_1236+125insG MANE Select	ENSP00000265517.5:n.1236+124_1236+125insG
ENST00000457717.6:c.1236+124_1236+125insG	ENSP00000400821.1:n.1236+124_1236+125insG
ENST00000511045.6:c.987+124_987+125insG	ENSP00000427679.2:n.987+124_987+125insG
ENST00000265517.9:c.1236+124_1236+125insG	ENSP00000265517.5:n.1236+124_1236+125insG
ENST00000457717.5:c.1236+124_1236+125insG	ENSP00000400821.1:n.1236+124_1236+125insG
ENST00000511045.5:c.1317+124_1317+125insG	ENSP00000427679.1:n.1317+124_1317+125insG
ENST00000619629.1:c.1236+124_1236+125insG	ENSP00000482850.1:n.1236+124_1236+125insG
NM_000253.3:c.1236+124_1236+125insG	NP_000244.2:n.1236+124_1236+125insG
NM_001300785.1:c.1317+124_1317+125insG	NP_001287714.1:n.1317+124_1317+125insG
NM_000253.4:c.1236+124_1236+125insG	NP_000244.2:n.1236+124_1236+125insG
NM_001300785.2:c.987+124_987+125insG	NP_001287714.2:n.987+124_987+125insG
NM_001386140.1:c.1236+124_1236+125insG MANE Select	NP_001373069.1:n.1236+124_1236+125insG