Canonical Allele Identifier: CA505174236
Gene: TICAM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4816590C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4816578C>G , CM000681.2:g.4816578C>G GRCh38
NC_000019.9:g.4816590C>G , CM000681.1:g.4816590C>G GRCh37
NC_000019.8:g.4767590C>G NCBI36
NG_031998.1:g.20165G>C , LRG_358:g.20165G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248244.6:c.1800G>C MANE Select ENSP00000248244.4:p.Gly600=
ENST00000248244.5:c.1800G>C ENSP00000248244.4:p.Gly600=
ENST00000621756.1:c.1383G>C ENSP00000479467.1:p.Gly461=
NM_182919.3:c.1800G>C , LRG_358t1:c.1800G>C NP_891549.1:p.Gly600=
NM_001385678.1:c.1758G>C NP_001372607.1:p.Gly586=
NM_001385679.1:c.1665G>C NP_001372608.1:p.Gly555=
NM_001385680.1:c.1158G>C NP_001372609.1:p.Gly386=
NM_182919.4:c.1800G>C MANE Select NP_891549.1:p.Gly600=