Canonical Allele Identifier: CA645617168
Gene: GATA1 HGNC NCBI

Linked Data

COSMIC: COSM18040

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48791271_48791287del , CM000685.2:g.48791271_48791287del GRCh38
NC_000023.10:g.48649678_48649694del , CM000685.1:g.48649678_48649694del GRCh37
NC_000023.9:g.48534622_48534638del NCBI36
NG_008846.2:g.9698_9714del , LRG_559:g.9698_9714del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651144.2:c.-29-573_-29-557del ENSP00000498550.1:n.-29-573_-29-557del
ENST00000696450.1:c.162_178del ENSP00000512637.1:p.Ala55GlyfsTer7
ENST00000696451.1:c.-29-573_-29-557del ENSP00000512638.1:n.-29-573_-29-557del
ENST00000696452.1:c.-29-573_-29-557del ENSP00000512639.1:n.-29-573_-29-557del
ENST00000376670.9:c.162_178del MANE Select ENSP00000365858.3:p.Ala55GlyfsTer7
ENST00000651144.1:c.-29-573_-29-557del ENSP00000498550.1:n.-29-573_-29-557del
ENST00000376665.4:c.162_178del ENSP00000365853.3:p.Ala55GlyfsTer7
ENST00000376670.7:c.162_178del ENSP00000365858.3:p.Ala55GlyfsTer7
NM_002049.3:c.162_178del , LRG_559t1:c.162_178del NP_002040.1:p.Ala55GlyfsTer7
XM_011543897.1:c.162_178del XP_011542199.1:p.Ala55GlyfsTer7
XM_011543898.1:c.-29-573_-29-557del XP_011542200.1:n.-29-573_-29-557del
XM_011543897.2:c.162_178del XP_011542199.1:p.Ala55GlyfsTer7
XM_011543898.2:c.-29-573_-29-557del XP_011542200.1:n.-29-573_-29-557del
XM_024452363.1:c.-29-573_-29-557del XP_024308131.1:n.-29-573_-29-557del
NM_002049.4:c.162_178del MANE Select NP_002040.1:p.Ala55GlyfsTer7