Canonical Allele Identifier: CA1480079196

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99600715_99600718delinsACTC , CM000666.2:g.99600715_99600718delinsACTC	GRCh38
NC_000004.11:g.100521872_100521875delinsACTC , CM000666.1:g.100521872_100521875delinsACTC	GRCh37
NC_000004.10:g.100740895_100740898delinsACTC	NCBI36
NG_011469.1:g.41633_41636delinsACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.1218_1221delinsACTC MANE Select	ENSP00000265517.5:p.Glu406=
ENST00000457717.6:c.1218_1221delinsACTC	ENSP00000400821.1:p.Glu406=
ENST00000511045.6:c.969_972delinsACTC	ENSP00000427679.2:p.Glu323=
ENST00000265517.9:c.1218_1221delinsACTC	ENSP00000265517.5:p.Glu406=
ENST00000457717.5:c.1218_1221delinsACTC	ENSP00000400821.1:p.Glu406=
ENST00000511045.5:c.1299_1302delinsACTC	ENSP00000427679.1:p.Glu433=
ENST00000619629.1:c.1218_1221delinsACTC	ENSP00000482850.1:p.Glu406=
NM_000253.3:c.1218_1221delinsACTC	NP_000244.2:p.Glu406=
NM_001300785.1:c.1299_1302delinsACTC	NP_001287714.1:p.Glu433=
NM_000253.4:c.1218_1221delinsACTC	NP_000244.2:p.Glu406=
NM_001300785.2:c.969_972delinsACTC	NP_001287714.2:p.Glu323=
NM_001386140.1:c.1218_1221delinsACTC MANE Select	NP_001373069.1:p.Glu406=