Canonical Allele Identifier: CA2321174065
Gene: TIMM44 HGNC NCBI

Linked Data

dbSNP Id: rs1984367391
gnomAD v4: 19-7943535-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7943535G>A , CM000681.2:g.7943535G>A GRCh38
NC_000019.9:g.8008420G>A , CM000681.1:g.8008420G>A GRCh37
NC_000019.8:g.7914420G>A NCBI36
NG_051180.1:g.5289C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000270538.8:c.45+72C>T MANE Select ENSP00000270538.2:n.45+72C>T
ENST00000270538.7:c.45+72C>T ENSP00000270538.2:n.45+72C>T
ENST00000595831.5:c.29+72C>T
ENST00000595876.5:c.45+72C>T ENSP00000471596.1:n.45+72C>T
ENST00000597926.1:c.45+72C>T ENSP00000469389.1:n.45+72C>T
ENST00000600000.1:n.60+72C>T
ENST00000600748.5:n.30+72C>T
NM_006351.3:c.45+72C>T NP_006342.2:n.45+72C>T
NM_006351.4:c.45+72C>T MANE Select NP_006342.2:n.45+72C>T