Canonical Allele Identifier: CA2428390675
Gene: GATA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48792464G= , CM000685.2:g.48792464G= GRCh38
NC_000023.10:g.48650871G= , CM000685.1:g.48650871G= GRCh37
NC_000023.9:g.48535815G= NCBI36
NG_008846.2:g.10891G= , LRG_559:g.10891G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651144.2:c.491G= ENSP00000498550.1:p.Arg164=
ENST00000696450.1:c.740G= ENSP00000512637.1:p.Arg247=
ENST00000696451.1:c.491G= ENSP00000512638.1:p.Arg164=
ENST00000696452.1:c.491G= ENSP00000512639.1:p.Arg164=
ENST00000376670.9:c.740G= MANE Select ENSP00000365858.3:p.Arg247=
ENST00000651144.1:c.491G= ENSP00000498550.1:p.Arg164=
ENST00000376665.4:c.740G= ENSP00000365853.3:p.Arg247=
ENST00000376670.7:c.740G= ENSP00000365858.3:p.Arg247=
NM_002049.3:c.740G= , LRG_559t1:c.740G= NP_002040.1:p.Arg247=
XM_011543897.1:c.740G= XP_011542199.1:p.Arg247=
XM_011543898.1:c.491G= XP_011542200.1:p.Arg164=
XM_011543897.2:c.740G= XP_011542199.1:p.Arg247=
XM_011543898.2:c.491G= XP_011542200.1:p.Arg164=
XM_024452363.1:c.491G= XP_024308131.1:p.Arg164=
NM_002049.4:c.740G= MANE Select NP_002040.1:p.Arg247=