Canonical Allele Identifier: CA360838771

Gene: HINT1

Linked Data

• MyVariant Identifiers: chr5:g.130498321C>T (hg19) ; chr5:g.131162628C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131162628C>T , CM000667.2:g.131162628C>T	GRCh38
NC_000005.9:g.130498321C>T , CM000667.1:g.130498321C>T	GRCh37
NC_000005.8:g.130526220C>T	NCBI36
NG_032998.1:g.7721G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304043.10:c.160G>A MANE Select	ENSP00000304229.5:p.Val54Met
ENST00000506207.2:n.285G>A
ENST00000506908.2:c.160G>A	ENSP00000426860.1:p.Val54Met
ENST00000508488.2:c.160G>A	ENSP00000427499.1:p.Val54Met
ENST00000511475.6:c.160G>A	ENSP00000427008.1:p.Val54Met
ENST00000513012.2:c.195G>A	ENSP00000422444.1:p.Trp65Ter
ENST00000513345.6:c.195G>A	ENSP00000421608.1:p.Trp65Ter
ENST00000520028.2:c.160G>A	ENSP00000430909.2:p.Val54Met
ENST00000675100.1:c.160G>A	ENSP00000502350.1:p.Val54Met
ENST00000675135.1:n.519G>A
ENST00000675372.1:c.195G>A	ENSP00000502792.1:p.Trp65Ter
ENST00000675491.1:c.160G>A	ENSP00000502370.1:p.Val54Met
ENST00000676117.1:n.241G>A
ENST00000304043.9:c.160G>A	ENSP00000304229.5:p.Val54Met
ENST00000504202.1:c.195G>A	ENSP00000425260.1:p.Trp65Ter
ENST00000506207.1:n.179G>A
ENST00000506908.1:c.160G>A	ENSP00000426860.1:p.Val54Met
ENST00000508488.1:c.160G>A	ENSP00000427499.1:p.Val54Met
ENST00000508495.5:c.160G>A	ENSP00000424974.1:p.Val54Met
ENST00000511475.5:c.160G>A	ENSP00000427008.1:p.Val54Met
ENST00000513012.1:c.195G>A	ENSP00000422444.1:p.Trp65Ter
ENST00000513345.5:c.195G>A	ENSP00000421608.1:p.Trp65Ter
NM_005340.6:c.160G>A	NP_005331.1:p.Val54Met
NR_024610.2:n.303G>A
NR_024611.2:n.338G>A
NR_073488.1:n.338G>A
XM_011543356.1:c.160G>A	XP_011541658.1:p.Val54Met
NR_134494.1:n.303G>A
NR_134495.1:n.303G>A
NM_005340.7:c.160G>A MANE Select	NP_005331.1:p.Val54Met
NR_024610.3:n.211G>A
NR_024611.3:n.246G>A
NR_073488.2:n.246G>A
NR_134494.2:n.211G>A
NR_134495.2:n.211G>A