Canonical Allele Identifier: CA370149374

Gene: SHH

Linked Data

• MyVariant Identifiers: chr7:g.155599214A>G (hg19) ; chr7:g.155806520A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.155806520A>G , CM000669.2:g.155806520A>G	GRCh38
NC_000007.13:g.155599214A>G , CM000669.1:g.155599214A>G	GRCh37
NC_000007.12:g.155291975A>G	NCBI36
NG_007504.2:g.10754T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297261.7:c.338T>C MANE Select	ENSP00000297261.2:p.Val113Ala
ENST00000297261.6:c.338T>C	ENSP00000297261.2:p.Val113Ala
ENST00000430104.5:c.77T>C	ENSP00000396621.1:p.Val26Ala
ENST00000435425.1:c.77T>C	ENSP00000413871.1:p.Val26Ala
ENST00000441114.5:c.77T>C	ENSP00000410546.1:p.Val26Ala
NM_000193.2:c.338T>C	NP_000184.1:p.Val113Ala
NM_000193.3:c.338T>C	NP_000184.1:p.Val113Ala
NM_001310462.1:c.77T>C	NP_001297391.1:p.Val26Ala
NR_132318.1:n.247T>C
NR_132319.1:n.247T>C
XM_011516479.1:c.77T>C	XP_011514781.1:p.Val26Ala
XM_011516480.1:c.77T>C	XP_011514782.1:p.Val26Ala
XM_011516481.1:c.77T>C	XP_011514783.1:p.Val26Ala
XM_011516482.1:c.-2T>C	XP_011514784.1:n.-2T>C
XM_011516479.2:c.77T>C	XP_011514781.1:p.Val26Ala
XM_011516480.2:c.77T>C	XP_011514782.1:p.Val26Ala
NM_000193.4:c.338T>C MANE Select	NP_000184.1:p.Val113Ala
NM_001310462.2:c.77T>C	NP_001297391.1:p.Val26Ala
NR_132318.2:n.338T>C
NR_132319.2:n.338T>C