Canonical Allele Identifier: CA1591234033

Gene: TNIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151085080A= , CM000667.2:g.151085080A=	GRCh38
NC_000005.9:g.150464641A= , CM000667.1:g.150464641A=	GRCh37
NC_000005.8:g.150444834A=	NCBI36
NG_030590.1:g.7581T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001252390.1:c.-37+2511T=	NP_001239319.1:n.-37+2511T=
NM_001252390.2:c.-37+2511T=	NP_001239319.1:n.-37+2511T=
NM_001252391.1:c.-37+2005T=	NP_001239320.1:n.-37+2005T=
NM_001252391.2:c.-37+2005T=	NP_001239320.1:n.-37+2005T=
NM_001252392.1:c.-37+2005T=	NP_001239321.1:n.-37+2005T=
NM_001252392.2:c.-37+2005T=	NP_001239321.1:n.-37+2005T=
ENST00000315050.11:c.-37+2005T=	ENSP00000317891.7:n.-37+2005T=
ENST00000521001.1:c.-37+8358T=	ENSP00000428404.1:n.-37+8358T=
ENST00000522100.5:c.-24+2005T=	ENSP00000428487.1:n.-24+2005T=
ENST00000522226.5:c.-37+2511T=	ENSP00000428187.1:n.-37+2511T=
ENST00000523338.5:c.-37+2005T=	ENSP00000428243.1:n.-37+2005T=
XM_017008946.2:c.-37+2005T=	XP_016864435.1:n.-37+2005T=
XM_017008947.2:c.-4273T=	XP_016864436.1:n.-4273T=