Canonical Allele Identifier: CA1866544742
Gene: TMOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97513142C= , CM000671.2:g.97513142C= GRCh38
NC_000009.11:g.100275424C= , CM000671.1:g.100275424C= GRCh37
NC_000009.10:g.99315245C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_003275.4:c.-48-10999C= MANE Select NP_003266.1:n.-48-10999C=
ENST00000259365.9:c.-48-10999C= MANE Select ENSP00000259365.3:n.-48-10999C=
NM_001166116.1:c.-48-10999C= NP_001159588.1:n.-48-10999C=
NM_001166116.2:c.-48-10999C= NP_001159588.1:n.-48-10999C=
NM_003275.3:c.-48-10999C= NP_003266.1:n.-48-10999C=
ENST00000259365.8:c.-48-10999C= ENSP00000259365.3:n.-48-10999C=
ENST00000395211.6:c.-48-10999C= ENSP00000378637.2:n.-48-10999C=
XM_024447660.1:c.-299-10999C= XP_024303428.1:n.-299-10999C=
XR_930157.1:n.902G=
XR_930157.2:n.827G=