Canonical Allele Identifier: CA10184884

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30615768A>C , CM000684.2:g.30615768A>C	GRCh38
NC_000022.10:g.31011755A>C , CM000684.1:g.31011755A>C	GRCh37
NC_000022.9:g.29341755A>C	NCBI36
NG_007263.1:g.13595A>C , LRG_116:g.13595A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.921A>C MANE Select	NP_000346.2:p.Pro307=
ENST00000215838.8:c.921A>C MANE Select	ENSP00000215838.3:p.Pro307=
NM_000355.3:c.921A>C	NP_000346.2:p.Pro307=
NM_001184726.1:c.840A>C	NP_001171655.1:p.Pro280=
NM_001184726.2:c.840A>C	NP_001171655.1:p.Pro280=
ENST00000215838.7:c.921A>C	ENSP00000215838.3:p.Pro307=
ENST00000405742.7:c.909A>C	ENSP00000385914.3:p.Pro303=
ENST00000407817.3:c.840A>C	ENSP00000384914.3:p.Pro280=
ENST00000450638.5:c.846A>C	ENSP00000394184.2:p.Pro282=
ENST00000471659.1:n.77A>C
ENST00000471659.2:n.2398A>C
ENST00000493542.1:n.53A>C
ENST00000698263.1:c.921A>C	ENSP00000513635.1:p.Pro307=
ENST00000698264.1:n.2398A>C
ENST00000698265.1:c.921A>C	ENSP00000513636.1:p.Pro307=
ENST00000698266.1:c.921A>C	ENSP00000513637.1:p.Pro307=
ENST00000698267.1:c.921A>C	ENSP00000513638.1:p.Pro307=
ENST00000698268.1:c.921A>C	ENSP00000513639.1:p.Pro307=
ENST00000698269.1:c.*487A>C	ENSP00000513640.1:n.*487A>C
ENST00000698270.1:c.768A>C	ENSP00000513641.1:p.Pro256=
ENST00000698271.1:c.951A>C	ENSP00000513642.1:p.Pro317=
ENST00000698272.1:c.912A>C	ENSP00000513643.1:p.Pro304=
ENST00000698273.1:c.912A>C	ENSP00000513644.1:p.Pro304=