Canonical Allele Identifier: CA2838232848
Gene: SASH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.148459697A>G , CM000668.2:g.148459697A>G GRCh38
NC_000006.11:g.148780833A>G , CM000668.1:g.148780833A>G GRCh37
NC_000006.10:g.148822526A>G NCBI36
NG_051927.1:g.192422A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367467.8:c.387-8848A>G MANE Select ENSP00000356437.3:n.387-8848A>G
ENST00000637469.1:c.32-8848A>G
ENST00000367467.7:c.387-8848A>G ENSP00000356437.3:n.387-8848A>G
ENST00000470750.1:n.51-8848A>G
NM_015278.3:c.387-8848A>G NP_056093.3:n.387-8848A>G
XM_005266874.3:c.495-8848A>G XP_005266931.1:n.495-8848A>G
XM_006715406.2:c.351-8848A>G XP_006715469.1:n.351-8848A>G
XM_011535637.1:c.384-8848A>G XP_011533939.1:n.384-8848A>G
XM_011535638.1:c.360-8848A>G XP_011533940.1:n.360-8848A>G
XM_011535639.1:c.276-8848A>G XP_011533941.1:n.276-8848A>G
XM_011535640.1:c.252-8848A>G XP_011533942.1:n.252-8848A>G
NM_001346505.1:c.252-8848A>G NP_001333434.1:n.252-8848A>G
NM_001346506.1:c.15-8848A>G NP_001333435.1:n.15-8848A>G
NM_015278.4:c.387-8848A>G NP_056093.3:n.387-8848A>G
XM_017010598.2:c.387-8848A>G XP_016866087.1:n.387-8848A>G
XM_017010599.1:c.276-8848A>G XP_016866088.1:n.276-8848A>G
XM_017010600.1:c.252-8848A>G XP_016866089.1:n.252-8848A>G
XM_017010605.1:c.15-8848A>G XP_016866094.1:n.15-8848A>G
XM_024446384.1:c.276-8848A>G XP_024302152.1:n.276-8848A>G
NM_015278.5:c.387-8848A>G MANE Select NP_056093.3:n.387-8848A>G
NM_001346505.2:c.252-8848A>G NP_001333434.1:n.252-8848A>G
NM_001346506.2:c.15-8848A>G NP_001333435.1:n.15-8848A>G