Canonical Allele Identifier: CA1754768195

Gene: SHH

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.155803294A= , CM000669.2:g.155803294A=	GRCh38
NC_000007.13:g.155595988A= , CM000669.1:g.155595988A=	GRCh37
NC_000007.12:g.155288749A=	NCBI36
NG_007504.2:g.13980T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000193.4:c.995T= MANE Select	NP_000184.1:p.Val332=
ENST00000297261.7:c.995T= MANE Select	ENSP00000297261.2:p.Val332=
NM_000193.2:c.995T=	NP_000184.1:p.Val332=
NM_000193.3:c.995T=	NP_000184.1:p.Val332=
NM_001310462.1:c.301+3002T=	NP_001297391.1:n.301+3002T=
NM_001310462.2:c.301+3002T=	NP_001297391.1:n.301+3002T=
NR_132318.1:n.472-2627T=
NR_132318.2:n.563-2627T=
NR_132319.1:n.472-2697T=
NR_132319.2:n.563-2697T=
ENST00000297261.6:c.995T=	ENSP00000297261.2:p.Val332=
ENST00000430104.5:c.301+3002T=	ENSP00000396621.1:n.301+3002T=
ENST00000435425.1:c.302-2697T=	ENSP00000413871.1:n.302-2697T=
ENST00000441114.5:c.302-2627T=	ENSP00000410546.1:n.302-2627T=
XM_011516479.1:c.734T=	XP_011514781.1:p.Val245=
XM_011516479.2:c.734T=	XP_011514781.1:p.Val245=
XM_011516480.1:c.734T=	XP_011514782.1:p.Val245=
XM_011516480.2:c.734T=	XP_011514782.1:p.Val245=
XM_011516481.1:c.734T=	XP_011514783.1:p.Val245=
XM_011516482.1:c.656T=	XP_011514784.1:p.Val219=