Canonical Allele Identifier: CA516029828

Gene: GATA1

Linked Data

• MyVariant Identifiers: chrX:g.48649693A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48791286A>G , CM000685.2:g.48791286A>G	GRCh38
NC_000023.10:g.48649693A>G , CM000685.1:g.48649693A>G	GRCh37
NC_000023.9:g.48534637A>G	NCBI36
NG_008846.2:g.9713A>G , LRG_559:g.9713A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000651144.2:c.-29-558A>G	ENSP00000498550.1:n.-29-558A>G
ENST00000696450.1:c.177A>G	ENSP00000512637.1:p.Ala59=
ENST00000696451.1:c.-29-558A>G	ENSP00000512638.1:n.-29-558A>G
ENST00000696452.1:c.-29-558A>G	ENSP00000512639.1:n.-29-558A>G
ENST00000376670.9:c.177A>G MANE Select	ENSP00000365858.3:p.Ala59=
ENST00000651144.1:c.-29-558A>G	ENSP00000498550.1:n.-29-558A>G
ENST00000376665.4:c.177A>G	ENSP00000365853.3:p.Ala59=
ENST00000376670.7:c.177A>G	ENSP00000365858.3:p.Ala59=
NM_002049.3:c.177A>G , LRG_559t1:c.177A>G	NP_002040.1:p.Ala59=
XM_011543897.1:c.177A>G	XP_011542199.1:p.Ala59=
XM_011543898.1:c.-29-558A>G	XP_011542200.1:n.-29-558A>G
XM_011543897.2:c.177A>G	XP_011542199.1:p.Ala59=
XM_011543898.2:c.-29-558A>G	XP_011542200.1:n.-29-558A>G
XM_024452363.1:c.-29-558A>G	XP_024308131.1:n.-29-558A>G
NM_002049.4:c.177A>G MANE Select	NP_002040.1:p.Ala59=