Canonical Allele Identifier: CA1883830901

Gene: SOHLH1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135699341G= , CM000671.2:g.135699341G=	GRCh38
NC_000009.11:g.138591187G= , CM000671.1:g.138591187G=	GRCh37
NC_000009.10:g.137731008G=	NCBI36
NG_033070.1:g.2157G=
NG_033784.1:g.5188C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000425225.2:c.65+62C= MANE Select	ENSP00000404438.1:n.65+62C=
ENST00000674066.1:n.1217-215C=
ENST00000298466.9:c.65+62C=	ENSP00000298466.5:n.65+62C=
ENST00000425225.1:c.65+62C=	ENSP00000404438.1:n.65+62C=
NM_001012415.2:c.65+62C=	NP_001012415.2:n.65+62C=
NM_001101677.1:c.65+62C=	NP_001095147.1:n.65+62C=
XM_005263403.2:c.65+62C=	XP_005263460.1:n.65+62C=
XM_006717109.2:c.-139-215C=	XP_006717172.1:n.-139-215C=
XM_011518698.1:c.65+62C=	XP_011517000.1:n.65+62C=
XM_005263403.3:c.65+62C=	XP_005263460.1:n.65+62C=
XM_006717109.4:c.-139-215C=	XP_006717172.1:n.-139-215C=
XM_011518698.3:c.65+62C=	XP_011517000.1:n.65+62C=
XM_024447552.1:c.-139-215C=	XP_024303320.1:n.-139-215C=
NM_001012415.3:c.65+62C=	NP_001012415.3:n.65+62C=
NM_001101677.2:c.65+62C= MANE Select	NP_001095147.2:n.65+62C=