Canonical Allele Identifier: CA323246003

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30626275G>T , CM000684.2:g.30626275G>T	GRCh38
NC_000022.10:g.31022262G>T , CM000684.1:g.31022262G>T	GRCh37
NC_000022.9:g.29352262G>T	NCBI36
NG_007263.1:g.24102G>T , LRG_116:g.24102G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.1223-185G>T MANE Select	NP_000346.2:n.1223-185G>T
ENST00000215838.8:c.1223-185G>T MANE Select	ENSP00000215838.3:n.1223-185G>T
NM_000355.3:c.1223-185G>T	NP_000346.2:n.1223-185G>T
NM_001184726.1:c.1142-185G>T	NP_001171655.1:n.1142-185G>T
NM_001184726.2:c.1142-185G>T	NP_001171655.1:n.1142-185G>T
ENST00000215838.7:c.1223-185G>T	ENSP00000215838.3:n.1223-185G>T
ENST00000405742.7:c.1211-185G>T	ENSP00000385914.3:n.1211-185G>T
ENST00000407817.3:c.1142-185G>T	ENSP00000384914.3:n.1142-185G>T
ENST00000450638.5:c.1148-185G>T	ENSP00000394184.2:n.1148-185G>T
ENST00000471659.2:n.3314-185G>T
ENST00000698263.1:c.1107-185G>T	ENSP00000513635.1:n.1107-185G>T
ENST00000698264.1:n.2959-185G>T
ENST00000698265.1:c.1208-185G>T	ENSP00000513636.1:n.1208-185G>T
ENST00000698266.1:c.*49-185G>T	ENSP00000513637.1:n.*49-185G>T
ENST00000698267.1:c.*79-185G>T	ENSP00000513638.1:n.*79-185G>T
ENST00000698268.1:c.1250-185G>T	ENSP00000513639.1:n.1250-185G>T
ENST00000698269.1:c.*789-185G>T	ENSP00000513640.1:n.*789-185G>T
ENST00000698270.1:c.1070-185G>T	ENSP00000513641.1:n.1070-185G>T
ENST00000698271.1:c.1253-185G>T	ENSP00000513642.1:n.1253-185G>T
ENST00000698272.1:c.1214-185G>T	ENSP00000513643.1:n.1214-185G>T
ENST00000698273.1:c.1214-185G>T	ENSP00000513644.1:n.1214-185G>T