Canonical Allele Identifier: CA516030351

Gene: GATA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48794068C>T , CM000685.2:g.48794068C>T	GRCh38
NC_000023.10:g.48652475C>T , CM000685.1:g.48652475C>T	GRCh37
NC_000023.9:g.48537419C>T	NCBI36
NG_008846.2:g.12495C>T , LRG_559:g.12495C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651144.2:c.897C>T	ENSP00000498550.1:p.Phe299=
ENST00000696450.1:c.1161C>T	ENSP00000512637.1:p.Phe387=
ENST00000696451.1:c.912C>T	ENSP00000512638.1:p.Phe304=
ENST00000696452.1:c.936C>T	ENSP00000512639.1:p.Phe312=
ENST00000376670.9:c.1146C>T MANE Select	ENSP00000365858.3:p.Phe382=
ENST00000651144.1:c.897C>T	ENSP00000498550.1:p.Phe299=
ENST00000376665.4:c.871-66C>T	ENSP00000365853.3:n.871-66C>T
ENST00000376670.7:c.1146C>T	ENSP00000365858.3:p.Phe382=
NM_002049.3:c.1146C>T , LRG_559t1:c.1146C>T	NP_002040.1:p.Phe382=
XM_011543897.1:c.1161C>T	XP_011542199.1:p.Phe387=
XM_011543898.1:c.912C>T	XP_011542200.1:p.Phe304=
XM_011543897.2:c.1161C>T	XP_011542199.1:p.Phe387=
XM_011543898.2:c.912C>T	XP_011542200.1:p.Phe304=
XM_024452363.1:c.897C>T	XP_024308131.1:p.Phe299=
NM_002049.4:c.1146C>T MANE Select	NP_002040.1:p.Phe382=