Canonical Allele Identifier: CA505174282
Gene: TICAM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4817001G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4816989G>C , CM000681.2:g.4816989G>C GRCh38
NC_000019.9:g.4817001G>C , CM000681.1:g.4817001G>C GRCh37
NC_000019.8:g.4768001G>C NCBI36
NG_031998.1:g.19754C>G , LRG_358:g.19754C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248244.6:c.1389C>G MANE Select ENSP00000248244.4:p.Arg463=
ENST00000248244.5:c.1389C>G ENSP00000248244.4:p.Arg463=
ENST00000621756.1:c.972C>G ENSP00000479467.1:p.Arg324=
NM_182919.3:c.1389C>G , LRG_358t1:c.1389C>G NP_891549.1:p.Arg463=
NM_001385678.1:c.1347C>G NP_001372607.1:p.Arg449=
NM_001385679.1:c.1254C>G NP_001372608.1:p.Arg418=
NM_001385680.1:c.747C>G NP_001372609.1:p.Arg249=
NM_182919.4:c.1389C>G MANE Select NP_891549.1:p.Arg463=