Canonical Allele Identifier: CA1883830912

Gene: SOHLH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135699356A= , CM000671.2:g.135699356A=	GRCh38
NC_000009.11:g.138591202A= , CM000671.1:g.138591202A=	GRCh37
NC_000009.10:g.137731023A=	NCBI36
NG_033070.1:g.2172A=
NG_033784.1:g.5173T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425225.2:c.65+47T= MANE Select	ENSP00000404438.1:n.65+47T=
ENST00000674066.1:n.1217-230T=
ENST00000298466.9:c.65+47T=	ENSP00000298466.5:n.65+47T=
ENST00000425225.1:c.65+47T=	ENSP00000404438.1:n.65+47T=
NM_001012415.2:c.65+47T=	NP_001012415.2:n.65+47T=
NM_001101677.1:c.65+47T=	NP_001095147.1:n.65+47T=
XM_005263403.2:c.65+47T=	XP_005263460.1:n.65+47T=
XM_006717109.2:c.-139-230T=	XP_006717172.1:n.-139-230T=
XM_011518698.1:c.65+47T=	XP_011517000.1:n.65+47T=
XM_005263403.3:c.65+47T=	XP_005263460.1:n.65+47T=
XM_006717109.4:c.-139-230T=	XP_006717172.1:n.-139-230T=
XM_011518698.3:c.65+47T=	XP_011517000.1:n.65+47T=
XM_024447552.1:c.-139-230T=	XP_024303320.1:n.-139-230T=
NM_001012415.3:c.65+47T=	NP_001012415.3:n.65+47T=
NM_001101677.2:c.65+47T= MANE Select	NP_001095147.2:n.65+47T=