Canonical Allele Identifier: CA74466853

Gene: TCAIM

Linked Data

• ClinVar Variation Id: 2552921
• ClinVar RCV Id: RCV004326402
• dbSNP Id: rs888077386
• MyVariant Identifiers: chr3:g.44437917C>T (hg19) ; chr3:g.44396425C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.44396425C>T , CM000665.2:g.44396425C>T	GRCh38
NC_000003.11:g.44437917C>T , CM000665.1:g.44437917C>T	GRCh37
NC_000003.10:g.44412921C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342649.9:c.721C>T MANE Select	ENSP00000341539.4:p.His241Tyr
ENST00000342649.8:c.721C>T	ENSP00000341539.4:p.His241Tyr
ENST00000412611.6:c.*297C>T	ENSP00000392032.2:n.*297C>T
ENST00000417237.5:c.721C>T	ENSP00000402581.1:p.His241Tyr
ENST00000417768.1:c.*297C>T	ENSP00000402604.1:n.*297C>T
ENST00000431657.5:c.*421C>T	ENSP00000387842.1:n.*421C>T
NM_001282913.1:c.721C>T	NP_001269842.1:p.His241Tyr
NM_001282914.1:c.289C>T	NP_001269843.1:p.His97Tyr
NM_001282915.1:c.289C>T	NP_001269844.1:p.His97Tyr
NM_173826.3:c.721C>T	NP_776187.2:p.His241Tyr
XM_011533621.1:c.289C>T	XP_011531923.1:p.His97Tyr
XR_001740117.2:n.2055C>T
XR_001740118.2:n.2527C>T
NM_173826.4:c.721C>T MANE Select	NP_776187.2:p.His241Tyr
NM_001282913.2:c.721C>T	NP_001269842.1:p.His241Tyr
NM_001282914.2:c.289C>T	NP_001269843.1:p.His97Tyr
NM_001282915.2:c.289C>T	NP_001269844.1:p.His97Tyr