Canonical Allele Identifier: CA15994783

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30623248A>C , CM000684.2:g.30623248A>C	GRCh38
NC_000022.10:g.31019235A>C , CM000684.1:g.31019235A>C	GRCh37
NC_000022.9:g.29349235A>C	NCBI36
NG_007263.1:g.21075A>C , LRG_116:g.21075A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.1222+165A>C MANE Select	NP_000346.2:n.1222+165A>C
ENST00000215838.8:c.1222+165A>C MANE Select	ENSP00000215838.3:n.1222+165A>C
NM_000355.3:c.1222+165A>C	NP_000346.2:n.1222+165A>C
NM_001184726.1:c.1141+165A>C	NP_001171655.1:n.1141+165A>C
NM_001184726.2:c.1141+165A>C	NP_001171655.1:n.1141+165A>C
ENST00000215838.7:c.1222+165A>C	ENSP00000215838.3:n.1222+165A>C
ENST00000405742.7:c.1210+165A>C	ENSP00000385914.3:n.1210+165A>C
ENST00000407817.3:c.1141+165A>C	ENSP00000384914.3:n.1141+165A>C
ENST00000450638.5:c.1147+165A>C	ENSP00000394184.2:n.1147+165A>C
ENST00000471659.2:n.3313+165A>C
ENST00000493542.1:n.519A>C
ENST00000698263.1:c.1107-3212A>C	ENSP00000513635.1:n.1107-3212A>C
ENST00000698264.1:n.2958+165A>C
ENST00000698265.1:c.1207+165A>C	ENSP00000513636.1:n.1207+165A>C
ENST00000698266.1:c.1222+165A>C	ENSP00000513637.1:n.1222+165A>C
ENST00000698267.1:c.*78+165A>C	ENSP00000513638.1:n.*78+165A>C
ENST00000698268.1:c.1249+165A>C	ENSP00000513639.1:n.1249+165A>C
ENST00000698269.1:c.*788+165A>C	ENSP00000513640.1:n.*788+165A>C
ENST00000698270.1:c.1069+165A>C	ENSP00000513641.1:n.1069+165A>C
ENST00000698271.1:c.1252+165A>C	ENSP00000513642.1:n.1252+165A>C
ENST00000698272.1:c.1213+165A>C	ENSP00000513643.1:n.1213+165A>C
ENST00000698273.1:c.1213+165A>C	ENSP00000513644.1:n.1213+165A>C