Canonical Allele Identifier: CA1883830969

Gene: SOHLH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135699442T= , CM000671.2:g.135699442T=	GRCh38
NC_000009.11:g.138591288T= , CM000671.1:g.138591288T=	GRCh37
NC_000009.10:g.137731109T=	NCBI36
NG_033070.1:g.2258T=
NG_033784.1:g.5087A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425225.2:c.26A= MANE Select	ENSP00000404438.1:p.Tyr9=
ENST00000674066.1:n.1217-316A=
ENST00000298466.9:c.26A=	ENSP00000298466.5:p.Tyr9=
ENST00000425225.1:c.26A=	ENSP00000404438.1:p.Tyr9=
NM_001012415.2:c.26A=	NP_001012415.2:p.Tyr9=
NM_001101677.1:c.26A=	NP_001095147.1:p.Tyr9=
XM_005263403.2:c.26A=	XP_005263460.1:p.Tyr9=
XM_006717109.2:c.-139-316A=	XP_006717172.1:n.-139-316A=
XM_011518698.1:c.26A=	XP_011517000.1:p.Tyr9=
XM_005263403.3:c.26A=	XP_005263460.1:p.Tyr9=
XM_006717109.4:c.-139-316A=	XP_006717172.1:n.-139-316A=
XM_011518698.3:c.26A=	XP_011517000.1:p.Tyr9=
XM_024447552.1:c.-139-316A=	XP_024303320.1:n.-139-316A=
NM_001012415.3:c.26A=	NP_001012415.3:p.Tyr9=
NM_001101677.2:c.26A= MANE Select	NP_001095147.2:p.Tyr9=