Canonical Allele Identifier: CA2693649559
Gene: GATA1 HGNC NCBI

Linked Data

gnomAD v4: X-48792293-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48792293A>C , CM000685.2:g.48792293A>C GRCh38
NC_000023.10:g.48650700A>C , CM000685.1:g.48650700A>C GRCh37
NC_000023.9:g.48535644A>C NCBI36
NG_008846.2:g.10720A>C , LRG_559:g.10720A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651144.2:c.350-30A>C ENSP00000498550.1:n.350-30A>C
ENST00000696450.1:c.599-30A>C ENSP00000512637.1:n.599-30A>C
ENST00000696451.1:c.350-30A>C ENSP00000512638.1:n.350-30A>C
ENST00000696452.1:c.350-30A>C ENSP00000512639.1:n.350-30A>C
ENST00000376670.9:c.599-30A>C MANE Select ENSP00000365858.3:n.599-30A>C
ENST00000651144.1:c.350-30A>C ENSP00000498550.1:n.350-30A>C
ENST00000376665.4:c.599-30A>C ENSP00000365853.3:n.599-30A>C
ENST00000376670.7:c.599-30A>C ENSP00000365858.3:n.599-30A>C
NM_002049.3:c.599-30A>C , LRG_559t1:c.599-30A>C NP_002040.1:n.599-30A>C
XM_011543897.1:c.599-30A>C XP_011542199.1:n.599-30A>C
XM_011543898.1:c.350-30A>C XP_011542200.1:n.350-30A>C
XM_011543897.2:c.599-30A>C XP_011542199.1:n.599-30A>C
XM_011543898.2:c.350-30A>C XP_011542200.1:n.350-30A>C
XM_024452363.1:c.350-30A>C XP_024308131.1:n.350-30A>C
NM_002049.4:c.599-30A>C MANE Select NP_002040.1:n.599-30A>C