Canonical Allele Identifier: CA516029857
Community Standard Title: NM_002049.4(GATA1):c.219A>G (p.Pro73=)
Gene: GATA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48791328A>G , CM000685.2:g.48791328A>G GRCh38
NC_000023.10:g.48649735A>G , CM000685.1:g.48649735A>G GRCh37
NC_000023.9:g.48534679A>G NCBI36
NG_008846.2:g.9755A>G , LRG_559:g.9755A>G

Transcript Alleles

HGVS Amino-acid Change
NM_002049.4:c.219A>G MANE Select NP_002040.1:p.Pro73=
ENST00000376670.9:c.219A>G MANE Select ENSP00000365858.3:p.Pro73=
NM_002049.3:c.219A>G , LRG_559t1:c.219A>G NP_002040.1:p.Pro73=
ENST00000376665.4:c.219A>G ENSP00000365853.3:p.Pro73=
ENST00000376670.7:c.219A>G ENSP00000365858.3:p.Pro73=
ENST00000651144.1:c.-29-516A>G ENSP00000498550.1:n.-29-516A>G
ENST00000651144.2:c.-29-516A>G ENSP00000498550.1:n.-29-516A>G
ENST00000696450.1:c.219A>G ENSP00000512637.1:p.Pro73=
ENST00000696451.1:c.-29-516A>G ENSP00000512638.1:n.-29-516A>G
ENST00000696452.1:c.-29-516A>G ENSP00000512639.1:n.-29-516A>G
XM_011543897.1:c.219A>G XP_011542199.1:p.Pro73=
XM_011543897.2:c.219A>G XP_011542199.1:p.Pro73=
XM_011543898.1:c.-29-516A>G XP_011542200.1:n.-29-516A>G
XM_011543898.2:c.-29-516A>G XP_011542200.1:n.-29-516A>G
XM_024452363.1:c.-29-516A>G XP_024308131.1:n.-29-516A>G