Canonical Allele Identifier: CA2428390271
Gene: GATA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48791283G= , CM000685.2:g.48791283G= GRCh38
NC_000023.10:g.48649690G= , CM000685.1:g.48649690G= GRCh37
NC_000023.9:g.48534634G= NCBI36
NG_008846.2:g.9710G= , LRG_559:g.9710G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651144.2:c.-29-561G= ENSP00000498550.1:n.-29-561G=
ENST00000696450.1:c.174G= ENSP00000512637.1:p.Ala58=
ENST00000696451.1:c.-29-561G= ENSP00000512638.1:n.-29-561G=
ENST00000696452.1:c.-29-561G= ENSP00000512639.1:n.-29-561G=
ENST00000376670.9:c.174G= MANE Select ENSP00000365858.3:p.Ala58=
ENST00000651144.1:c.-29-561G= ENSP00000498550.1:n.-29-561G=
ENST00000376665.4:c.174G= ENSP00000365853.3:p.Ala58=
ENST00000376670.7:c.174G= ENSP00000365858.3:p.Ala58=
NM_002049.3:c.174G= , LRG_559t1:c.174G= NP_002040.1:p.Ala58=
XM_011543897.1:c.174G= XP_011542199.1:p.Ala58=
XM_011543898.1:c.-29-561G= XP_011542200.1:n.-29-561G=
XM_011543897.2:c.174G= XP_011542199.1:p.Ala58=
XM_011543898.2:c.-29-561G= XP_011542200.1:n.-29-561G=
XM_024452363.1:c.-29-561G= XP_024308131.1:n.-29-561G=
NM_002049.4:c.174G= MANE Select NP_002040.1:p.Ala58=