Canonical Allele Identifier: CA3398665

Gene: HINT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131165149A>G , CM000667.2:g.131165149A>G	GRCh38
NC_000005.9:g.130500842A>G , CM000667.1:g.130500842A>G	GRCh37
NC_000005.8:g.130528741A>G	NCBI36
NG_032998.1:g.5200T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304043.10:c.57T>C MANE Select	ENSP00000304229.5:p.Phe19=
ENST00000506207.2:n.237-2473T>C
ENST00000506908.2:c.57T>C	ENSP00000426860.1:p.Phe19=
ENST00000508488.2:c.57T>C	ENSP00000427499.1:p.Phe19=
ENST00000511475.6:c.57T>C	ENSP00000427008.1:p.Phe19=
ENST00000513012.2:c.57T>C	ENSP00000422444.1:p.Phe19=
ENST00000513345.6:c.57T>C	ENSP00000421608.1:p.Phe19=
ENST00000520028.2:c.57T>C	ENSP00000430909.2:p.Phe19=
ENST00000675100.1:c.57T>C	ENSP00000502350.1:p.Phe19=
ENST00000675372.1:c.57T>C	ENSP00000502792.1:p.Phe19=
ENST00000675491.1:c.57T>C	ENSP00000502370.1:p.Phe19=
ENST00000304043.9:c.57T>C	ENSP00000304229.5:p.Phe19=
ENST00000504202.1:c.57T>C	ENSP00000425260.1:p.Phe19=
ENST00000506207.1:n.131-2473T>C
ENST00000506908.1:c.57T>C	ENSP00000426860.1:p.Phe19=
ENST00000508488.1:c.57T>C	ENSP00000427499.1:p.Phe19=
ENST00000508495.5:c.57T>C	ENSP00000424974.1:p.Phe19=
ENST00000511475.5:c.57T>C	ENSP00000427008.1:p.Phe19=
ENST00000513012.1:c.57T>C	ENSP00000422444.1:p.Phe19=
ENST00000513345.5:c.57T>C	ENSP00000421608.1:p.Phe19=
NM_005340.6:c.57T>C	NP_005331.1:p.Phe19=
NR_024610.2:n.200T>C
NR_024611.2:n.200T>C
NR_073488.1:n.200T>C
XM_011543356.1:c.57T>C	XP_011541658.1:p.Phe19=
NR_134494.1:n.200T>C
NR_134495.1:n.200T>C
NM_005340.7:c.57T>C MANE Select	NP_005331.1:p.Phe19=
NR_024610.3:n.108T>C
NR_024611.3:n.108T>C
NR_073488.2:n.108T>C
NR_134494.2:n.108T>C
NR_134495.2:n.108T>C