Canonical Allele Identifier: CA323235155

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30617411C>T , CM000684.2:g.30617411C>T	GRCh38
NC_000022.10:g.31013398C>T , CM000684.1:g.31013398C>T	GRCh37
NC_000022.9:g.29343398C>T	NCBI36
NG_007263.1:g.15238C>T , LRG_116:g.15238C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000355.4:c.1022C>T MANE Select	NP_000346.2:p.Pro341Leu
ENST00000215838.8:c.1022C>T MANE Select	ENSP00000215838.3:p.Pro341Leu
NM_000355.3:c.1022C>T	NP_000346.2:p.Pro341Leu
NM_001184726.1:c.941C>T	NP_001171655.1:p.Pro314Leu
NM_001184726.2:c.941C>T	NP_001171655.1:p.Pro314Leu
ENST00000215838.7:c.1022C>T	ENSP00000215838.3:p.Pro341Leu
ENST00000405742.7:c.1010C>T	ENSP00000385914.3:p.Pro337Leu
ENST00000407817.3:c.941C>T	ENSP00000384914.3:p.Pro314Leu
ENST00000450638.5:c.947C>T	ENSP00000394184.2:p.Pro316Leu
ENST00000471659.1:n.178C>T
ENST00000471659.2:n.2499C>T
ENST00000493542.1:n.154C>T
ENST00000698263.1:c.1022C>T	ENSP00000513635.1:p.Pro341Leu
ENST00000698264.1:n.2499C>T
ENST00000698265.1:c.1022C>T	ENSP00000513636.1:p.Pro341Leu
ENST00000698266.1:c.1022C>T	ENSP00000513637.1:p.Pro341Leu
ENST00000698267.1:c.940+1624C>T	ENSP00000513638.1:n.940+1624C>T
ENST00000698268.1:c.1049C>T	ENSP00000513639.1:p.Pro350Leu
ENST00000698269.1:c.*588C>T	ENSP00000513640.1:n.*588C>T
ENST00000698270.1:c.869C>T	ENSP00000513641.1:p.Pro290Leu
ENST00000698271.1:c.1052C>T	ENSP00000513642.1:p.Pro351Leu
ENST00000698272.1:c.1013C>T	ENSP00000513643.1:p.Pro338Leu
ENST00000698273.1:c.1013C>T	ENSP00000513644.1:p.Pro338Leu