Canonical Allele Identifier: CA12063511

Gene: HINT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131164755G>C , CM000667.2:g.131164755G>C	GRCh38
NC_000005.9:g.130500448G>C , CM000667.1:g.130500448G>C	GRCh37
NC_000005.8:g.130528347G>C	NCBI36
NG_032998.1:g.5594C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005340.7:c.111+340C>G MANE Select	NP_005331.1:n.111+340C>G
ENST00000304043.10:c.111+340C>G MANE Select	ENSP00000304229.5:n.111+340C>G
NM_005340.6:c.111+340C>G	NP_005331.1:n.111+340C>G
NR_024610.2:n.254+340C>G
NR_024610.3:n.162+340C>G
NR_024611.2:n.289+305C>G
NR_024611.3:n.197+305C>G
NR_073488.1:n.289+305C>G
NR_073488.2:n.197+305C>G
NR_134494.1:n.254+340C>G
NR_134494.2:n.162+340C>G
NR_134495.1:n.254+340C>G
NR_134495.2:n.162+340C>G
ENST00000304043.9:c.111+340C>G	ENSP00000304229.5:n.111+340C>G
ENST00000504202.1:c.146+305C>G	ENSP00000425260.1:n.146+305C>G
ENST00000506207.1:n.131-2079C>G
ENST00000506207.2:n.237-2079C>G
ENST00000506908.1:c.111+340C>G	ENSP00000426860.1:n.111+340C>G
ENST00000506908.2:c.111+340C>G	ENSP00000426860.1:n.111+340C>G
ENST00000508488.1:c.111+340C>G	ENSP00000427499.1:n.111+340C>G
ENST00000508488.2:c.111+340C>G	ENSP00000427499.1:n.111+340C>G
ENST00000508495.5:c.111+340C>G	ENSP00000424974.1:n.111+340C>G
ENST00000511475.5:c.111+340C>G	ENSP00000427008.1:n.111+340C>G
ENST00000511475.6:c.111+340C>G	ENSP00000427008.1:n.111+340C>G
ENST00000513012.1:c.146+305C>G	ENSP00000422444.1:n.146+305C>G
ENST00000513012.2:c.146+305C>G	ENSP00000422444.1:n.146+305C>G
ENST00000513345.5:c.146+305C>G	ENSP00000421608.1:n.146+305C>G
ENST00000513345.6:c.146+305C>G	ENSP00000421608.1:n.146+305C>G
ENST00000520028.2:c.111+340C>G	ENSP00000430909.2:n.111+340C>G
ENST00000675100.1:c.111+340C>G	ENSP00000502350.1:n.111+340C>G
ENST00000675372.1:c.146+305C>G	ENSP00000502792.1:n.146+305C>G
ENST00000675491.1:c.111+340C>G	ENSP00000502370.1:n.111+340C>G
XM_011543356.1:c.111+340C>G	XP_011541658.1:n.111+340C>G