Canonical Allele Identifier: CA505174161
Gene: TICAM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4816788C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4816776C>T , CM000681.2:g.4816776C>T GRCh38
NC_000019.9:g.4816788C>T , CM000681.1:g.4816788C>T GRCh37
NC_000019.8:g.4767788C>T NCBI36
NG_031998.1:g.19967G>A , LRG_358:g.19967G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248244.6:c.1602G>A MANE Select ENSP00000248244.4:p.Gln534=
ENST00000248244.5:c.1602G>A ENSP00000248244.4:p.Gln534=
ENST00000621756.1:c.1185G>A ENSP00000479467.1:p.Gln395=
NM_182919.3:c.1602G>A , LRG_358t1:c.1602G>A NP_891549.1:p.Gln534=
NM_001385678.1:c.1560G>A NP_001372607.1:p.Gln520=
NM_001385679.1:c.1467G>A NP_001372608.1:p.Gln489=
NM_001385680.1:c.960G>A NP_001372609.1:p.Gln320=
NM_182919.4:c.1602G>A MANE Select NP_891549.1:p.Gln534=