Canonical Allele Identifier: CA412870721
Gene: GATA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48792386G>T , CM000685.2:g.48792386G>T GRCh38
NC_000023.10:g.48650793G>T , CM000685.1:g.48650793G>T GRCh37
NC_000023.9:g.48535737G>T NCBI36
NG_008846.2:g.10813G>T , LRG_559:g.10813G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651144.2:c.413G>T ENSP00000498550.1:p.Gly138Val
ENST00000696450.1:c.662G>T ENSP00000512637.1:p.Gly221Val
ENST00000696451.1:c.413G>T ENSP00000512638.1:p.Gly138Val
ENST00000696452.1:c.413G>T ENSP00000512639.1:p.Gly138Val
ENST00000376670.9:c.662G>T MANE Select ENSP00000365858.3:p.Gly221Val
ENST00000651144.1:c.413G>T ENSP00000498550.1:p.Gly138Val
ENST00000376665.4:c.662G>T ENSP00000365853.3:p.Gly221Val
ENST00000376670.7:c.662G>T ENSP00000365858.3:p.Gly221Val
NM_002049.3:c.662G>T , LRG_559t1:c.662G>T NP_002040.1:p.Gly221Val
XM_011543897.1:c.662G>T XP_011542199.1:p.Gly221Val
XM_011543898.1:c.413G>T XP_011542200.1:p.Gly138Val
XM_011543897.2:c.662G>T XP_011542199.1:p.Gly221Val
XM_011543898.2:c.413G>T XP_011542200.1:p.Gly138Val
XM_024452363.1:c.413G>T XP_024308131.1:p.Gly138Val
NM_002049.4:c.662G>T MANE Select NP_002040.1:p.Gly221Val