Canonical Allele Identifier: CA1455676935
Gene: TEC HGNC NCBI

Linked Data

dbSNP Id: rs1723163133

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.48218861T>C , CM000666.2:g.48218861T>C GRCh38
NC_000004.11:g.48220878T>C , CM000666.1:g.48220878T>C GRCh37
NC_000004.10:g.47915635T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381501.8:c.138+9616A>G MANE Select ENSP00000370912.3:n.138+9616A>G
ENST00000381501.7:c.138+9616A>G ENSP00000370912.3:n.138+9616A>G
ENST00000505452.5:c.138+9616A>G ENSP00000424567.1:n.138+9616A>G
NM_003215.2:c.138+9616A>G NP_003206.2:n.138+9616A>G
XM_011513735.1:c.138+9616A>G XP_011512037.1:n.138+9616A>G
XM_011513736.1:c.138+9616A>G XP_011512038.1:n.138+9616A>G
XM_011513737.1:c.-109+9616A>G XP_011512039.1:n.-109+9616A>G
XM_011513738.1:c.-143+9616A>G XP_011512040.1:n.-143+9616A>G
XM_011513739.1:c.-51+9616A>G XP_011512041.1:n.-51+9616A>G
XM_011513740.1:c.138+9616A>G XP_011512042.1:n.138+9616A>G
XM_011513741.1:c.138+9616A>G XP_011512043.1:n.138+9616A>G
XR_925160.1:n.183+9616A>G
XR_925161.1:n.183+9616A>G
XM_011513737.2:c.-109+9616A>G XP_011512039.1:n.-109+9616A>G
XM_024454193.1:c.138+9616A>G XP_024309961.1:n.138+9616A>G
XR_001741318.1:n.183+9616A>G
XR_001741319.1:n.296+9616A>G
XR_925160.2:n.183+9616A>G
NM_003215.3:c.138+9616A>G MANE Select NP_003206.2:n.138+9616A>G