Canonical Allele Identifier: CA1821070257

Gene: TG SLA

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133050021A>T , CM000670.2:g.133050021A>T	GRCh38
NC_000008.10:g.134062266A>T , CM000670.1:g.134062266A>T	GRCh37
NC_000008.9:g.134131448A>T	NCBI36
NG_015832.1:g.188062A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.7239+19998A>T (TG) MANE Select	ENSP00000220616.4:n.7239+19998A>T
ENST00000338087.10:c.162-33T>A (SLA) MANE Select	ENSP00000337548.5:n.162-33T>A
ENST00000220616.8:c.7239+19998A>T (TG)	ENSP00000220616.4:n.7239+19998A>T
ENST00000338087.9:c.162-33T>A (SLA)	ENSP00000337548.5:n.162-33T>A
ENST00000395352.7:c.213-33T>A (SLA)	ENSP00000378759.3:n.213-33T>A
ENST00000427060.6:c.282-33T>A (SLA)	ENSP00000394049.2:n.282-33T>A
ENST00000517648.5:c.213-33T>A (SLA)	ENSP00000428559.1:n.213-33T>A
ENST00000518565.5:n.526-33T>A (SLA)
ENST00000519178.5:c.2605+19998A>T (TG)
ENST00000519341.5:c.162-33T>A (SLA)	ENSP00000429681.1:n.162-33T>A
ENST00000519543.5:c.1638+19998A>T (TG)	ENSP00000430430.1:n.1638+19998A>T
ENST00000520106.5:n.377-33T>A (SLA)
ENST00000521823.5:n.455-33T>A (SLA)
ENST00000522002.5:n.303-33T>A (SLA)
ENST00000522119.5:c.162-33T>A (SLA)	ENSP00000430596.1:n.162-33T>A
ENST00000522432.5:c.*125-33T>A (SLA)	ENSP00000429844.1:n.*125-33T>A
ENST00000523224.5:n.299-33T>A (SLA)
ENST00000523756.5:c.3894+19998A>T (TG)
ENST00000524345.5:c.-163-33T>A (SLA)	ENSP00000427928.1:n.-163-33T>A
NM_001045556.2:c.162-33T>A (SLA)	NP_001039021.1:n.162-33T>A
NM_001045557.2:c.213-33T>A (SLA)	NP_001039022.2:n.213-33T>A
NM_001282964.1:c.213-33T>A (SLA)	NP_001269893.1:n.213-33T>A
NM_001282965.1:c.-163-33T>A (SLA)	NP_001269894.1:n.-163-33T>A
NM_003235.4:c.7239+19998A>T (TG)	NP_003226.4:n.7239+19998A>T
NM_006748.3:c.282-33T>A (SLA)	NP_006739.2:n.282-33T>A
XM_005251038.3:c.7047+19998A>T (TG)	XP_005251095.1:n.7047+19998A>T
XM_006716622.2:c.7176+19998A>T (TG)	XP_006716685.1:n.7176+19998A>T
XM_011517227.1:c.-163-33T>A (SLA)	XP_011515529.1:n.-163-33T>A
XM_005251038.4:c.7047+19998A>T (TG)	XP_005251095.1:n.7047+19998A>T
XM_006716622.3:c.7176+19998A>T (TG)	XP_006716685.1:n.7176+19998A>T
XM_017013739.2:c.-163-33T>A (SLA)	XP_016869228.1:n.-163-33T>A
XM_017013793.1:c.7173+19998A>T (TG)	XP_016869282.1:n.7173+19998A>T
XM_017013794.1:c.7239+19998A>T (TG)	XP_016869283.1:n.7239+19998A>T
XM_017013795.1:c.7068+19998A>T (TG)	XP_016869284.1:n.7068+19998A>T
XM_017013796.1:c.7020+19998A>T (TG)	XP_016869285.1:n.7020+19998A>T
XM_017013797.1:c.6978+19998A>T (TG)	XP_016869286.1:n.6978+19998A>T
XM_017013798.1:c.7239+19998A>T (TG)	XP_016869287.1:n.7239+19998A>T
NM_001045556.3:c.162-33T>A (SLA) MANE Select	NP_001039021.1:n.162-33T>A
NM_003235.5:c.7239+19998A>T (TG) MANE Select	NP_003226.4:n.7239+19998A>T
NM_001045557.3:c.213-33T>A (SLA)	NP_001039022.2:n.213-33T>A
NM_001282964.2:c.213-33T>A (SLA)	NP_001269893.1:n.213-33T>A
NM_001282965.2:c.-163-33T>A (SLA)	NP_001269894.1:n.-163-33T>A
NM_006748.4:c.282-33T>A (SLA)	NP_006739.2:n.282-33T>A