Canonical Allele Identifier: CA375965490

Gene: GATA3

Linked Data

• gnomAD v4: 10-8055836-C-G
• MyVariant Identifiers: chr10:g.8097799C>G (hg19) ; chr10:g.8055836C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8055836C>G , CM000672.2:g.8055836C>G	GRCh38
NC_000010.10:g.8097799C>G , CM000672.1:g.8097799C>G	GRCh37
NC_000010.9:g.8137805C>G	NCBI36
NG_015859.1:g.6133C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.181C>G	ENSP00000341619.3:p.Pro61Ala
ENST00000379328.9:c.181C>G MANE Select	ENSP00000368632.3:p.Pro61Ala
ENST00000481743.2:c.181C>G	ENSP00000493486.1:p.Pro61Ala
ENST00000643001.1:c.181C>G	ENSP00000494284.1:p.Pro61Ala
ENST00000346208.3:c.181C>G	ENSP00000341619.3:p.Pro61Ala
ENST00000379328.7:c.181C>G	ENSP00000368632.3:p.Pro61Ala
NM_001002295.1:c.181C>G	NP_001002295.1:p.Pro61Ala
NM_002051.2:c.181C>G	NP_002042.1:p.Pro61Ala
XM_005252442.2:c.181C>G	XP_005252499.1:p.Pro61Ala
XM_005252443.3:c.181C>G	XP_005252500.1:p.Pro61Ala
XM_005252443.5:c.181C>G	XP_005252500.1:p.Pro61Ala
XR_001747358.1:n.617+930G>C
NM_001002295.2:c.181C>G MANE Select	NP_001002295.1:p.Pro61Ala
NM_002051.3:c.181C>G	NP_002042.1:p.Pro61Ala