Canonical Allele Identifier: CA938481333

Gene: TCN1

Linked Data

• dbSNP Id: rs1853068480
• gnomAD v3: 11-59865953-A-G
• gnomAD v4: 11-59865953-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.59865953A>G , CM000673.2:g.59865953A>G	GRCh38
NC_000011.9:g.59633426A>G , CM000673.1:g.59633426A>G	GRCh37
NC_000011.8:g.59390002A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000257264.4:c.79+439T>C MANE Select	ENSP00000257264.3:n.79+439T>C
ENST00000257264.3:c.79+439T>C	ENSP00000257264.3:n.79+439T>C
ENST00000532419.5:n.98+439T>C
ENST00000534531.1:n.80+439T>C
NM_001062.3:c.79+439T>C	NP_001053.2:n.79+439T>C
NM_001062.4:c.79+439T>C MANE Select	NP_001053.2:n.79+439T>C