Canonical Allele Identifier: CA800728168

Gene: MTTP

Linked Data

• dbSNP Id: rs1457781968
• gnomAD v3: 4-99618749-A-ATC
• gnomAD v4: 4-99618749-A-ATC
• MyVariant Identifiers: chr4:g.100539906_100539907insTC (hg19) ; chr4:g.99618749_99618750insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99618750_99618751dup , CM000666.2:g.99618750_99618751dup	GRCh38
NC_000004.11:g.100539907_100539908dup , CM000666.1:g.100539907_100539908dup	GRCh37
NC_000004.10:g.100758930_100758931dup	NCBI36
NG_011469.1:g.59668_59669dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000265517.10:c.2218-224_2218-223dup MANE Select	ENSP00000265517.5:n.2218-224_2218-223dup
ENST00000457717.6:c.2218-224_2218-223dup	ENSP00000400821.1:n.2218-224_2218-223dup
ENST00000511045.6:c.1969-224_1969-223dup	ENSP00000427679.2:n.1969-224_1969-223dup
ENST00000265517.9:c.2218-224_2218-223dup	ENSP00000265517.5:n.2218-224_2218-223dup
ENST00000457717.5:c.2218-224_2218-223dup	ENSP00000400821.1:n.2218-224_2218-223dup
ENST00000511045.5:c.2299-224_2299-223dup	ENSP00000427679.1:n.2299-224_2299-223dup
ENST00000619629.1:c.*665-224_*665-223dup	ENSP00000482850.1:n.*665-224_*665-223dup
NM_000253.3:c.2218-224_2218-223dup	NP_000244.2:n.2218-224_2218-223dup
NM_001300785.1:c.2299-224_2299-223dup	NP_001287714.1:n.2299-224_2299-223dup
NM_000253.4:c.2218-224_2218-223dup	NP_000244.2:n.2218-224_2218-223dup
NM_001300785.2:c.1969-224_1969-223dup	NP_001287714.2:n.1969-224_1969-223dup
NM_001386140.1:c.2218-224_2218-223dup MANE Select	NP_001373069.1:n.2218-224_2218-223dup