Canonical Allele Identifier: CA9149807
Gene: TIMM44 HGNC NCBI

Linked Data

dbSNP Id: rs113707296
ExAC: 19:7998899 G / A
gnomAD v2: 19-7998899-G-A
gnomAD v3: 19-7934014-G-A
gnomAD v4: 19-7934014-G-A
MyVariant Identifiers: chr19:g.7998899G>A (hg19) chr19:g.7934014G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7934014G>A , CM000681.2:g.7934014G>A GRCh38
NC_000019.9:g.7998899G>A , CM000681.1:g.7998899G>A GRCh37
NC_000019.8:g.7904899G>A NCBI36
NG_051180.1:g.14810C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000270538.8:c.544-11C>T MANE Select ENSP00000270538.2:n.544-11C>T
ENST00000270538.7:c.544-11C>T ENSP00000270538.2:n.544-11C>T
ENST00000595831.5:c.531-11C>T
ENST00000595876.5:c.*232-11C>T ENSP00000471596.1:n.*232-11C>T
ENST00000597926.1:c.448-11C>T ENSP00000469389.1:n.448-11C>T
ENST00000600748.5:n.529-11C>T
NM_006351.3:c.544-11C>T NP_006342.2:n.544-11C>T
NM_006351.4:c.544-11C>T MANE Select NP_006342.2:n.544-11C>T
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