Canonical Allele Identifier: CA2671535564

Gene: MTTP

Linked Data

• gnomAD v4: 4-99622911-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622911A>C , CM000666.2:g.99622911A>C	GRCh38
NC_000004.11:g.100544068A>C , CM000666.1:g.100544068A>C	GRCh37
NC_000004.10:g.100763091A>C	NCBI36
NG_011469.1:g.63829A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.*63A>C MANE Select	ENSP00000265517.5:n.*63A>C
ENST00000457717.6:c.*63A>C	ENSP00000400821.1:n.*63A>C
ENST00000511045.6:c.*63A>C	ENSP00000427679.2:n.*63A>C
ENST00000265517.9:c.*63A>C	ENSP00000265517.5:n.*63A>C
ENST00000457717.5:c.*63A>C	ENSP00000400821.1:n.*63A>C
ENST00000511045.5:c.*63A>C	ENSP00000427679.1:n.*63A>C
ENST00000619629.1:c.*1195A>C	ENSP00000482850.1:n.*1195A>C
NM_000253.3:c.*63A>C	NP_000244.2:n.*63A>C
NM_001300785.1:c.*63A>C	NP_001287714.1:n.*63A>C
NM_000253.4:c.*63A>C	NP_000244.2:n.*63A>C
NM_001300785.2:c.*63A>C	NP_001287714.2:n.*63A>C
NM_001386140.1:c.*63A>C MANE Select	NP_001373069.1:n.*63A>C