Canonical Allele Identifier: CA412870576

Gene: GATA1

Linked Data

• MyVariant Identifiers: chrX:g.48650766C>G (hg19) ; chrX:g.48792359C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48792359C>G , CM000685.2:g.48792359C>G	GRCh38
NC_000023.10:g.48650766C>G , CM000685.1:g.48650766C>G	GRCh37
NC_000023.9:g.48535710C>G	NCBI36
NG_008846.2:g.10786C>G , LRG_559:g.10786C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651144.2:c.386C>G	ENSP00000498550.1:p.Thr129Ser
ENST00000696450.1:c.635C>G	ENSP00000512637.1:p.Thr212Ser
ENST00000696451.1:c.386C>G	ENSP00000512638.1:p.Thr129Ser
ENST00000696452.1:c.386C>G	ENSP00000512639.1:p.Thr129Ser
ENST00000376670.9:c.635C>G MANE Select	ENSP00000365858.3:p.Thr212Ser
ENST00000651144.1:c.386C>G	ENSP00000498550.1:p.Thr129Ser
ENST00000376665.4:c.635C>G	ENSP00000365853.3:p.Thr212Ser
ENST00000376670.7:c.635C>G	ENSP00000365858.3:p.Thr212Ser
NM_002049.3:c.635C>G , LRG_559t1:c.635C>G	NP_002040.1:p.Thr212Ser
XM_011543897.1:c.635C>G	XP_011542199.1:p.Thr212Ser
XM_011543898.1:c.386C>G	XP_011542200.1:p.Thr129Ser
XM_011543897.2:c.635C>G	XP_011542199.1:p.Thr212Ser
XM_011543898.2:c.386C>G	XP_011542200.1:p.Thr129Ser
XM_024452363.1:c.386C>G	XP_024308131.1:p.Thr129Ser
NM_002049.4:c.635C>G MANE Select	NP_002040.1:p.Thr212Ser