Canonical Allele Identifier: CA652201255

Gene: GATA4

Linked Data

• gnomAD v4: 8-11758645-G-T
• COSMIC: COSN26638143

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11758645G>T , CM000670.2:g.11758645G>T	GRCh38
NC_000008.10:g.11616154G>T , CM000670.1:g.11616154G>T	GRCh37
NC_000008.9:g.11653563G>T	NCBI36
NG_008177.2:g.86727G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622443.3:c.*170G>T	ENSP00000482268.2:n.*170G>T
ENST00000532059.6:c.*170G>T MANE Select	ENSP00000435712.1:n.*170G>T
ENST00000335135.8:c.*170G>T	ENSP00000334458.4:n.*170G>T
ENST00000526021.1:n.944G>T
ENST00000528712.5:c.*170G>T	ENSP00000435043.1:n.*170G>T
ENST00000622443.2:c.1496G>T	ENSP00000482268.1:n.1496G>T
NM_001308093.1:c.*170G>T	NP_001295022.1:n.*170G>T
NM_001308094.1:c.*170G>T	NP_001295023.1:n.*170G>T
NM_002052.3:c.*170G>T	NP_002043.2:n.*170G>T
NM_002052.4:c.*170G>T	NP_002043.2:n.*170G>T
XM_005272385.3:c.*170G>T	XP_005272442.1:n.*170G>T
XM_005272386.1:c.*170G>T	XP_005272443.1:n.*170G>T
XM_006716248.1:c.*170G>T	XP_006716311.1:n.*170G>T
XM_011543817.1:c.*170G>T	XP_011542119.1:n.*170G>T
XM_011543818.1:c.*170G>T	XP_011542120.1:n.*170G>T
XM_005272385.4:c.*170G>T	XP_005272442.1:n.*170G>T
XM_011543817.3:c.*170G>T	XP_011542119.1:n.*170G>T
XM_011543818.2:c.*170G>T	XP_011542120.1:n.*170G>T
XM_017013312.2:c.*170G>T	XP_016868801.1:n.*170G>T
NM_001308093.3:c.*170G>T MANE Select	NP_001295022.1:n.*170G>T
NM_001308094.2:c.*170G>T	NP_001295023.1:n.*170G>T
NM_001374273.1:c.*170G>T	NP_001361202.1:n.*170G>T
NM_001374274.1:c.*170G>T	NP_001361203.1:n.*170G>T
NM_002052.5:c.*170G>T	NP_002043.2:n.*170G>T