Canonical Allele Identifier: CA412870965

Gene: GATA1

Linked Data

• MyVariant Identifiers: chrX:g.48650837G>C (hg19) ; chrX:g.48792430G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48792430G>C , CM000685.2:g.48792430G>C	GRCh38
NC_000023.10:g.48650837G>C , CM000685.1:g.48650837G>C	GRCh37
NC_000023.9:g.48535781G>C	NCBI36
NG_008846.2:g.10857G>C , LRG_559:g.10857G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651144.2:c.457G>C	ENSP00000498550.1:p.Gly153Arg
ENST00000696450.1:c.706G>C	ENSP00000512637.1:p.Gly236Arg
ENST00000696451.1:c.457G>C	ENSP00000512638.1:p.Gly153Arg
ENST00000696452.1:c.457G>C	ENSP00000512639.1:p.Gly153Arg
ENST00000376670.9:c.706G>C MANE Select	ENSP00000365858.3:p.Gly236Arg
ENST00000651144.1:c.457G>C	ENSP00000498550.1:p.Gly153Arg
ENST00000376665.4:c.706G>C	ENSP00000365853.3:p.Gly236Arg
ENST00000376670.7:c.706G>C	ENSP00000365858.3:p.Gly236Arg
NM_002049.3:c.706G>C , LRG_559t1:c.706G>C	NP_002040.1:p.Gly236Arg
XM_011543897.1:c.706G>C	XP_011542199.1:p.Gly236Arg
XM_011543898.1:c.457G>C	XP_011542200.1:p.Gly153Arg
XM_011543897.2:c.706G>C	XP_011542199.1:p.Gly236Arg
XM_011543898.2:c.457G>C	XP_011542200.1:p.Gly153Arg
XM_024452363.1:c.457G>C	XP_024308131.1:p.Gly153Arg
NM_002049.4:c.706G>C MANE Select	NP_002040.1:p.Gly236Arg