Canonical Allele Identifier: CA1671522927

Gene: SASH1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.148466870C= , CM000668.2:g.148466870C=	GRCh38
NC_000006.11:g.148788006C= , CM000668.1:g.148788006C=	GRCh37
NC_000006.10:g.148829699C=	NCBI36
NG_051927.1:g.199595C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015278.5:c.387-1675C= MANE Select	NP_056093.3:n.387-1675C=
ENST00000367467.8:c.387-1675C= MANE Select	ENSP00000356437.3:n.387-1675C=
NM_001346505.1:c.252-1675C=	NP_001333434.1:n.252-1675C=
NM_001346505.2:c.252-1675C=	NP_001333434.1:n.252-1675C=
NM_001346506.1:c.15-1675C=	NP_001333435.1:n.15-1675C=
NM_001346506.2:c.15-1675C=	NP_001333435.1:n.15-1675C=
NM_015278.3:c.387-1675C=	NP_056093.3:n.387-1675C=
NM_015278.4:c.387-1675C=	NP_056093.3:n.387-1675C=
ENST00000367467.7:c.387-1675C=	ENSP00000356437.3:n.387-1675C=
ENST00000470750.1:n.51-1675C=
ENST00000637469.1:c.32-1675C=
XM_005266874.3:c.495-1675C=	XP_005266931.1:n.495-1675C=
XM_006715406.2:c.351-1675C=	XP_006715469.1:n.351-1675C=
XM_011535637.1:c.384-1675C=	XP_011533939.1:n.384-1675C=
XM_011535638.1:c.360-1675C=	XP_011533940.1:n.360-1675C=
XM_011535639.1:c.276-1675C=	XP_011533941.1:n.276-1675C=
XM_011535640.1:c.252-1675C=	XP_011533942.1:n.252-1675C=
XM_017010598.2:c.387-1675C=	XP_016866087.1:n.387-1675C=
XM_017010599.1:c.276-1675C=	XP_016866088.1:n.276-1675C=
XM_017010600.1:c.252-1675C=	XP_016866089.1:n.252-1675C=
XM_017010605.1:c.15-1675C=	XP_016866094.1:n.15-1675C=
XM_024446384.1:c.276-1675C=	XP_024302152.1:n.276-1675C=