Canonical Allele Identifier: CA795534081

Gene: TEC

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.48195372A>T , CM000666.2:g.48195372A>T	GRCh38
NC_000004.11:g.48197389A>T , CM000666.1:g.48197389A>T	GRCh37
NC_000004.10:g.47892146A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381501.8:c.139-19186T>A MANE Select	ENSP00000370912.3:n.139-19186T>A
ENST00000381501.7:c.139-19186T>A	ENSP00000370912.3:n.139-19186T>A
ENST00000505452.5:c.139-19186T>A	ENSP00000424567.1:n.139-19186T>A
NM_003215.2:c.139-19186T>A	NP_003206.2:n.139-19186T>A
XM_011513735.1:c.139-19186T>A	XP_011512037.1:n.139-19186T>A
XM_011513736.1:c.139-19186T>A	XP_011512038.1:n.139-19186T>A
XM_011513737.1:c.30+2749T>A	XP_011512039.1:n.30+2749T>A
XM_011513738.1:c.30+2749T>A	XP_011512040.1:n.30+2749T>A
XM_011513739.1:c.30+2749T>A	XP_011512041.1:n.30+2749T>A
XM_011513740.1:c.139-19186T>A	XP_011512042.1:n.139-19186T>A
XM_011513741.1:c.139-19186T>A	XP_011512043.1:n.139-19186T>A
XR_925160.1:n.184-19186T>A
XR_925161.1:n.184-19186T>A
XM_011513737.2:c.30+2749T>A	XP_011512039.1:n.30+2749T>A
XM_017008569.1:c.-211+1253T>A	XP_016864058.1:n.-211+1253T>A
XM_024454193.1:c.139-19186T>A	XP_024309961.1:n.139-19186T>A
XR_001741318.1:n.184-19186T>A
XR_001741319.1:n.297-19186T>A
XR_925160.2:n.184-19186T>A
NM_003215.3:c.139-19186T>A MANE Select	NP_003206.2:n.139-19186T>A