Canonical Allele Identifier: CA129872149

Gene: TNIP1

Linked Data

• dbSNP Id: rs76956521
• gnomAD v3: 5-151085080-A-G
• gnomAD v4: 5-151085080-A-G
• MyVariant Identifiers: chr5:g.150464641A>G (hg19) ; chr5:g.151085080A>G (hg38)

Genomic Alleles

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

Transcript Alleles

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