Canonical Allele Identifier: CA10404696
Community Standard Title: NM_002049.4(GATA1):c.1067G>A (p.Gly356Asp)
Gene: GATA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48793989G>A , CM000685.2:g.48793989G>A GRCh38
NC_000023.10:g.48652396G>A , CM000685.1:g.48652396G>A GRCh37
NC_000023.9:g.48537340G>A NCBI36
NG_008846.2:g.12416G>A , LRG_559:g.12416G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002049.4:c.1067G>A MANE Select NP_002040.1:p.Gly356Asp
ENST00000376670.9:c.1067G>A MANE Select ENSP00000365858.3:p.Gly356Asp
NM_002049.3:c.1067G>A , LRG_559t1:c.1067G>A NP_002040.1:p.Gly356Asp
ENST00000376665.4:c.871-145G>A ENSP00000365853.3:n.871-145G>A
ENST00000376670.7:c.1067G>A ENSP00000365858.3:p.Gly356Asp
ENST00000651144.1:c.818G>A ENSP00000498550.1:p.Gly273Asp
ENST00000651144.2:c.818G>A ENSP00000498550.1:p.Gly273Asp
ENST00000696450.1:c.1082G>A ENSP00000512637.1:p.Gly361Asp
ENST00000696451.1:c.833G>A ENSP00000512638.1:p.Gly278Asp
ENST00000696452.1:c.857G>A ENSP00000512639.1:p.Gly286Asp
XM_011543897.1:c.1082G>A XP_011542199.1:p.Gly361Asp
XM_011543897.2:c.1082G>A XP_011542199.1:p.Gly361Asp
XM_011543898.1:c.833G>A XP_011542200.1:p.Gly278Asp
XM_011543898.2:c.833G>A XP_011542200.1:p.Gly278Asp
XM_024452363.1:c.818G>A XP_024308131.1:p.Gly273Asp