Canonical Allele Identifier: CA323234038

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30616048_30616075del , CM000684.2:g.30616048_30616075del	GRCh38
NC_000022.10:g.31012035_31012062del , CM000684.1:g.31012035_31012062del	GRCh37
NC_000022.9:g.29342035_29342062del	NCBI36
NG_007263.1:g.13875_13902del , LRG_116:g.13875_13902del

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.940+261_940+288del MANE Select	NP_000346.2:n.940+261_940+288del
ENST00000215838.8:c.940+261_940+288del MANE Select	ENSP00000215838.3:n.940+261_940+288del
NM_000355.3:c.940+261_940+288del	NP_000346.2:n.940+261_940+288del
NM_001184726.1:c.859+261_859+288del	NP_001171655.1:n.859+261_859+288del
NM_001184726.2:c.859+261_859+288del	NP_001171655.1:n.859+261_859+288del
ENST00000215838.7:c.940+261_940+288del	ENSP00000215838.3:n.940+261_940+288del
ENST00000405742.7:c.928+261_928+288del	ENSP00000385914.3:n.928+261_928+288del
ENST00000407817.3:c.859+261_859+288del	ENSP00000384914.3:n.859+261_859+288del
ENST00000450638.5:c.865+261_865+288del	ENSP00000394184.2:n.865+261_865+288del
ENST00000471659.1:n.96+261_96+288del
ENST00000471659.2:n.2417+261_2417+288del
ENST00000493542.1:n.72+261_72+288del
ENST00000698263.1:c.940+261_940+288del	ENSP00000513635.1:n.940+261_940+288del
ENST00000698264.1:n.2417+261_2417+288del
ENST00000698265.1:c.940+261_940+288del	ENSP00000513636.1:n.940+261_940+288del
ENST00000698266.1:c.940+261_940+288del	ENSP00000513637.1:n.940+261_940+288del
ENST00000698267.1:c.940+261_940+288del	ENSP00000513638.1:n.940+261_940+288del
ENST00000698268.1:c.940+261_940+288del	ENSP00000513639.1:n.940+261_940+288del
ENST00000698269.1:c.*506+261_*506+288del	ENSP00000513640.1:n.*506+261_*506+288del
ENST00000698270.1:c.787+261_787+288del	ENSP00000513641.1:n.787+261_787+288del
ENST00000698271.1:c.970+261_970+288del	ENSP00000513642.1:n.970+261_970+288del
ENST00000698272.1:c.931+261_931+288del	ENSP00000513643.1:n.931+261_931+288del
ENST00000698273.1:c.931+261_931+288del	ENSP00000513644.1:n.931+261_931+288del