Canonical Allele Identifier: CA505173832
Gene: TICAM1 HGNC NCBI

Linked Data

dbSNP Id: rs1600052306
gnomAD v3: 19-4816383-C-T
gnomAD v4: 19-4816383-C-T
MyVariant Identifiers: chr19:g.4816395C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4816383C>T , CM000681.2:g.4816383C>T GRCh38
NC_000019.9:g.4816395C>T , CM000681.1:g.4816395C>T GRCh37
NC_000019.8:g.4767395C>T NCBI36
NG_031998.1:g.20360G>A , LRG_358:g.20360G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248244.6:c.1995G>A MANE Select ENSP00000248244.4:p.Thr665=
ENST00000248244.5:c.1995G>A ENSP00000248244.4:p.Thr665=
ENST00000621756.1:c.1497G>A ENSP00000479467.1:p.Thr499=
NM_182919.3:c.1995G>A , LRG_358t1:c.1995G>A NP_891549.1:p.Thr665=
NM_001385678.1:c.1953G>A NP_001372607.1:p.Thr651=
NM_001385679.1:c.1860G>A NP_001372608.1:p.Thr620=
NM_001385680.1:c.1353G>A NP_001372609.1:p.Thr451=
NM_182919.4:c.1995G>A MANE Select NP_891549.1:p.Thr665=