Canonical Allele Identifier: CA10404675
Community Standard Title: NM_002049.4(GATA1):c.871-7T>C
Gene: GATA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48793786T>C , CM000685.2:g.48793786T>C GRCh38
NC_000023.10:g.48652193T>C , CM000685.1:g.48652193T>C GRCh37
NC_000023.9:g.48537137T>C NCBI36
NG_008846.2:g.12213T>C , LRG_559:g.12213T>C

Transcript Alleles

HGVS Amino-acid Change
NM_002049.4:c.871-7T>C MANE Select NP_002040.1:n.871-7T>C
ENST00000376670.9:c.871-7T>C MANE Select ENSP00000365858.3:n.871-7T>C
NM_002049.3:c.871-7T>C , LRG_559t1:c.871-7T>C NP_002040.1:n.871-7T>C
ENST00000376665.4:c.871-348T>C ENSP00000365853.3:n.871-348T>C
ENST00000376670.7:c.871-7T>C ENSP00000365858.3:n.871-7T>C
ENST00000651144.1:c.622-7T>C ENSP00000498550.1:n.622-7T>C
ENST00000651144.2:c.622-7T>C ENSP00000498550.1:n.622-7T>C
ENST00000696450.1:c.879T>C ENSP00000512637.1:p.Phe293=
ENST00000696451.1:c.630T>C ENSP00000512638.1:p.Phe210=
ENST00000696452.1:c.654T>C ENSP00000512639.1:p.Phe218=
XM_011543897.1:c.879T>C XP_011542199.1:p.Phe293=
XM_011543897.2:c.879T>C XP_011542199.1:p.Phe293=
XM_011543898.1:c.630T>C XP_011542200.1:p.Phe210=
XM_011543898.2:c.630T>C XP_011542200.1:p.Phe210=
XM_024452363.1:c.622-7T>C XP_024308131.1:n.622-7T>C