Canonical Allele Identifier: CA2838200154

Gene: TARBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.234468036G>A , CM000663.2:g.234468036G>A	GRCh38
NC_000001.10:g.234603782G>A , CM000663.1:g.234603782G>A	GRCh37
NC_000001.9:g.232670405G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000040877.2:c.1100-386C>T MANE Select	ENSP00000040877.1:n.1100-386C>T
ENST00000040877.1:c.1100-386C>T	ENSP00000040877.1:n.1100-386C>T
NM_005646.3:c.1100-386C>T	NP_005637.3:n.1100-386C>T
XM_005273234.2:c.1100-386C>T	XP_005273291.1:n.1100-386C>T
XM_011544263.1:c.1100-386C>T	XP_011542565.1:n.1100-386C>T
XM_011544264.1:c.1100-386C>T	XP_011542566.1:n.1100-386C>T
XM_011544265.1:c.1100-386C>T	XP_011542567.1:n.1100-386C>T
XR_949155.1:n.1152-386C>T
XR_949156.1:n.1153-386C>T
XR_949157.1:n.1153-386C>T
XR_949158.1:n.1155-386C>T
XM_005273234.3:c.1100-386C>T	XP_005273291.1:n.1100-386C>T
XM_011544263.2:c.1100-386C>T	XP_011542565.1:n.1100-386C>T
XM_017002194.2:c.1100-386C>T	XP_016857683.1:n.1100-386C>T
XM_017002195.1:c.-171-386C>T	XP_016857684.1:n.-171-386C>T
XM_017002197.1:c.-934-386C>T	XP_016857686.1:n.-934-386C>T
XR_001737374.1:n.1169-386C>T
XR_001737375.1:n.1170-386C>T
XR_001737376.2:n.1171-386C>T
XR_001737377.1:n.1171-386C>T
XR_001737378.2:n.1171-386C>T
XR_001737379.2:n.1171-386C>T
XR_001737380.2:n.1171-386C>T
XR_001737381.2:n.1170-386C>T
XR_001737382.2:n.1171-386C>T
XR_001737383.1:n.128-386C>T
XR_002957455.1:n.1169-386C>T
XR_002957456.1:n.1171-386C>T
XR_949155.2:n.1169-386C>T
XR_949157.2:n.1169-386C>T
XR_949158.3:n.1171-386C>T
NM_005646.4:c.1100-386C>T MANE Select	NP_005637.3:n.1100-386C>T