Canonical Allele Identifier: CA357501958

Gene: MTTP

Linked Data

• gnomAD v4: 4-99583380-G-T
• MyVariant Identifiers: chr4:g.100504537G>T (hg19) ; chr4:g.99583380G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583380G>T , CM000666.2:g.99583380G>T	GRCh38
NC_000004.11:g.100504537G>T , CM000666.1:g.100504537G>T	GRCh37
NC_000004.10:g.100723560G>T	NCBI36
NG_011469.1:g.24298G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.256G>T MANE Select	ENSP00000265517.5:p.Asp86Tyr
ENST00000457717.6:c.256G>T	ENSP00000400821.1:p.Asp86Tyr
ENST00000505094.6:c.7G>T	ENSP00000422782.2:p.Asp3Tyr
ENST00000511045.6:c.7G>T	ENSP00000427679.2:p.Asp3Tyr
ENST00000265517.9:c.256G>T	ENSP00000265517.5:p.Asp86Tyr
ENST00000422897.6:c.256G>T	ENSP00000407350.2:p.Asp86Tyr
ENST00000457717.5:c.256G>T	ENSP00000400821.1:p.Asp86Tyr
ENST00000505094.5:c.*346G>T	ENSP00000422782.1:n.*346G>T
ENST00000506883.5:c.286G>T	ENSP00000426755.1:p.Asp96Tyr
ENST00000511045.5:c.337G>T	ENSP00000427679.1:p.Asp113Tyr
ENST00000513404.5:c.*319G>T	ENSP00000424972.1:n.*319G>T
ENST00000515141.5:c.*319G>T	ENSP00000425642.1:n.*319G>T
ENST00000619629.1:c.256G>T	ENSP00000482850.1:p.Asp86Tyr
NM_000253.3:c.256G>T	NP_000244.2:p.Asp86Tyr
NM_001300785.1:c.337G>T	NP_001287714.1:p.Asp113Tyr
NM_000253.4:c.256G>T	NP_000244.2:p.Asp86Tyr
NM_001300785.2:c.7G>T	NP_001287714.2:p.Asp3Tyr
NM_001386140.1:c.256G>T MANE Select	NP_001373069.1:p.Asp86Tyr