Canonical Allele Identifier: CA1582590146

Gene: HINT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131161735T= , CM000667.2:g.131161735T=	GRCh38
NC_000005.9:g.130497428T= , CM000667.1:g.130497428T=	GRCh37
NC_000005.8:g.130525327T=	NCBI36
NG_032998.1:g.8614A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304043.10:c.216+837A= MANE Select	ENSP00000304229.5:n.216+837A=
ENST00000506207.2:n.341+837A=
ENST00000506908.2:c.*816A=	ENSP00000426860.1:n.*816A=
ENST00000508488.2:c.*318+329A=	ENSP00000427499.1:n.*318+329A=
ENST00000511475.6:c.*20+627A=	ENSP00000427008.1:n.*20+627A=
ENST00000513012.2:c.*890A=	ENSP00000422444.1:n.*890A=
ENST00000513345.6:c.*502+294A=	ENSP00000421608.1:n.*502+294A=
ENST00000520028.2:c.*415+294A=	ENSP00000430909.2:n.*415+294A=
ENST00000675100.1:c.216+837A=	ENSP00000502350.1:n.216+837A=
ENST00000675135.1:n.575+837A=
ENST00000675372.1:c.*53+837A=	ENSP00000502792.1:n.*53+837A=
ENST00000675491.1:c.*647A=	ENSP00000502370.1:n.*647A=
ENST00000676117.1:n.439+627A=
ENST00000304043.9:c.216+837A=	ENSP00000304229.5:n.216+837A=
ENST00000504202.1:c.*169+627A=	ENSP00000425260.1:n.*169+627A=
ENST00000506207.1:n.235+837A=
ENST00000508495.5:c.216+837A=	ENSP00000424974.1:n.216+837A=
ENST00000511475.5:c.*20+627A=	ENSP00000427008.1:n.*20+627A=
ENST00000513345.5:c.*53+837A=	ENSP00000421608.1:n.*53+837A=
NM_005340.6:c.216+837A=	NP_005331.1:n.216+837A=
NR_024610.2:n.359+837A=
NR_024611.2:n.394+837A=
NR_073488.1:n.510+627A=
NR_134494.1:n.475+627A=
NR_134495.1:n.808+294A=
NM_005340.7:c.216+837A= MANE Select	NP_005331.1:n.216+837A=
NR_024610.3:n.267+837A=
NR_024611.3:n.302+837A=
NR_073488.2:n.418+627A=
NR_134494.2:n.383+627A=
NR_134495.2:n.716+294A=