Canonical Allele Identifier: CA3398563

Gene: HINT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131159551C>A , CM000667.2:g.131159551C>A	GRCh38
NC_000005.9:g.130495244C>A , CM000667.1:g.130495244C>A	GRCh37
NC_000005.8:g.130523143C>A	NCBI36
NG_032998.1:g.10798G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005340.7:c.277G>T MANE Select	NP_005331.1:p.Gly93Cys
ENST00000304043.10:c.277G>T MANE Select	ENSP00000304229.5:p.Gly93Cys
NM_005340.6:c.277G>T	NP_005331.1:p.Gly93Cys
NR_024610.2:n.609G>T
NR_024610.3:n.517G>T
NR_024611.2:n.455G>T
NR_024611.3:n.363G>T
NR_073488.1:n.800G>T
NR_073488.2:n.708G>T
NR_134494.1:n.765G>T
NR_134494.2:n.673G>T
NR_134495.1:n.869G>T
NR_134495.2:n.777G>T
ENST00000304043.9:c.277G>T	ENSP00000304229.5:p.Gly93Cys
ENST00000506207.1:n.296G>T
ENST00000506207.2:n.402G>T
ENST00000506908.2:c.*3000G>T	ENSP00000426860.1:n.*3000G>T
ENST00000508488.2:c.*379G>T	ENSP00000427499.1:n.*379G>T
ENST00000508495.5:c.*229G>T	ENSP00000424974.1:n.*229G>T
ENST00000511475.5:c.*310G>T	ENSP00000427008.1:n.*310G>T
ENST00000511475.6:c.*310G>T	ENSP00000427008.1:n.*310G>T
ENST00000513012.2:c.*3074G>T	ENSP00000422444.1:n.*3074G>T
ENST00000513345.5:c.*114G>T	ENSP00000421608.1:n.*114G>T
ENST00000513345.6:c.*563G>T	ENSP00000421608.1:n.*563G>T
ENST00000520028.2:c.*476G>T	ENSP00000430909.2:n.*476G>T
ENST00000675100.1:c.216+3021G>T	ENSP00000502350.1:n.216+3021G>T
ENST00000675135.1:n.636G>T
ENST00000675372.1:c.*114G>T	ENSP00000502792.1:n.*114G>T
ENST00000675491.1:c.*2831G>T	ENSP00000502370.1:n.*2831G>T
ENST00000676117.1:n.729G>T