Canonical Allele Identifier: CA10404626

Gene: GATA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48792224G>A , CM000685.2:g.48792224G>A	GRCh38
NC_000023.10:g.48650631G>A , CM000685.1:g.48650631G>A	GRCh37
NC_000023.9:g.48535575G>A	NCBI36
NG_008846.2:g.10651G>A , LRG_559:g.10651G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002049.4:c.598+3G>A MANE Select	NP_002040.1:n.598+3G>A
ENST00000376670.9:c.598+3G>A MANE Select	ENSP00000365858.3:n.598+3G>A
NM_002049.3:c.598+3G>A , LRG_559t1:c.598+3G>A	NP_002040.1:n.598+3G>A
ENST00000376665.4:c.598+3G>A	ENSP00000365853.3:n.598+3G>A
ENST00000376670.7:c.598+3G>A	ENSP00000365858.3:n.598+3G>A
ENST00000651144.1:c.349+3G>A	ENSP00000498550.1:n.349+3G>A
ENST00000651144.2:c.349+3G>A	ENSP00000498550.1:n.349+3G>A
ENST00000696450.1:c.598+3G>A	ENSP00000512637.1:n.598+3G>A
ENST00000696451.1:c.349+3G>A	ENSP00000512638.1:n.349+3G>A
ENST00000696452.1:c.349+3G>A	ENSP00000512639.1:n.349+3G>A
XM_011543897.1:c.598+3G>A	XP_011542199.1:n.598+3G>A
XM_011543897.2:c.598+3G>A	XP_011542199.1:n.598+3G>A
XM_011543898.1:c.349+3G>A	XP_011542200.1:n.349+3G>A
XM_011543898.2:c.349+3G>A	XP_011542200.1:n.349+3G>A
XM_024452363.1:c.349+3G>A	XP_024308131.1:n.349+3G>A