Canonical Allele Identifier: CA1754768949

Gene: SHH

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.155803618A= , CM000669.2:g.155803618A=	GRCh38
NC_000007.13:g.155596312A= , CM000669.1:g.155596312A=	GRCh37
NC_000007.12:g.155289073A=	NCBI36
NG_007504.2:g.13656T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000193.4:c.671T= MANE Select	NP_000184.1:p.Val224=
ENST00000297261.7:c.671T= MANE Select	ENSP00000297261.2:p.Val224=
NM_000193.2:c.671T=	NP_000184.1:p.Val224=
NM_000193.3:c.671T=	NP_000184.1:p.Val224=
NM_001310462.1:c.301+2678T=	NP_001297391.1:n.301+2678T=
NM_001310462.2:c.301+2678T=	NP_001297391.1:n.301+2678T=
NR_132318.1:n.471+2678T=
NR_132318.2:n.562+2678T=
NR_132319.1:n.471+2678T=
NR_132319.2:n.562+2678T=
ENST00000297261.6:c.671T=	ENSP00000297261.2:p.Val224=
ENST00000430104.5:c.301+2678T=	ENSP00000396621.1:n.301+2678T=
ENST00000435425.1:c.301+2678T=	ENSP00000413871.1:n.301+2678T=
ENST00000441114.5:c.301+2678T=	ENSP00000410546.1:n.301+2678T=
XM_011516479.1:c.410T=	XP_011514781.1:p.Val137=
XM_011516479.2:c.410T=	XP_011514781.1:p.Val137=
XM_011516480.1:c.410T=	XP_011514782.1:p.Val137=
XM_011516480.2:c.410T=	XP_011514782.1:p.Val137=
XM_011516481.1:c.410T=	XP_011514783.1:p.Val137=
XM_011516482.1:c.332T=	XP_011514784.1:p.Val111=