Canonical Allele Identifier: CA360838038

Gene: HINT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131159460C>T , CM000667.2:g.131159460C>T	GRCh38
NC_000005.9:g.130495153C>T , CM000667.1:g.130495153C>T	GRCh37
NC_000005.8:g.130523052C>T	NCBI36
NG_032998.1:g.10889G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005340.7:c.368G>A MANE Select	NP_005331.1:p.Trp123Ter
ENST00000304043.10:c.368G>A MANE Select	ENSP00000304229.5:p.Trp123Ter
NM_005340.6:c.368G>A	NP_005331.1:p.Trp123Ter
NR_024610.2:n.700G>A
NR_024610.3:n.608G>A
NR_024611.2:n.546G>A
NR_024611.3:n.454G>A
NR_073488.1:n.891G>A
NR_073488.2:n.799G>A
NR_134494.1:n.856G>A
NR_134494.2:n.764G>A
NR_134495.1:n.960G>A
NR_134495.2:n.868G>A
ENST00000304043.9:c.368G>A	ENSP00000304229.5:p.Trp123Ter
ENST00000506908.2:c.*3091G>A	ENSP00000426860.1:n.*3091G>A
ENST00000508488.2:c.*470G>A	ENSP00000427499.1:n.*470G>A
ENST00000508495.5:c.*320G>A	ENSP00000424974.1:n.*320G>A
ENST00000511475.5:c.*401G>A	ENSP00000427008.1:n.*401G>A
ENST00000511475.6:c.*401G>A	ENSP00000427008.1:n.*401G>A
ENST00000513012.2:c.*3165G>A	ENSP00000422444.1:n.*3165G>A
ENST00000513345.5:c.*205G>A	ENSP00000421608.1:n.*205G>A
ENST00000513345.6:c.*654G>A	ENSP00000421608.1:n.*654G>A
ENST00000520028.2:c.*567G>A	ENSP00000430909.2:n.*567G>A
ENST00000675100.1:c.216+3112G>A	ENSP00000502350.1:n.216+3112G>A
ENST00000675135.1:n.727G>A
ENST00000675372.1:c.*205G>A	ENSP00000502792.1:n.*205G>A
ENST00000675491.1:c.*2922G>A	ENSP00000502370.1:n.*2922G>A
ENST00000676117.1:n.820G>A