Canonical Allele Identifier: CA2686137277

Gene: GATA4

Linked Data

• gnomAD v4: 8-11758193-C-CTAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11758193_11758194insTAGG , CM000670.2:g.11758193_11758194insTAGG	GRCh38
NC_000008.10:g.11615702_11615703insTAGG , CM000670.1:g.11615702_11615703insTAGG	GRCh37
NC_000008.9:g.11653111_11653112insTAGG	NCBI36
NG_008177.2:g.86275_86276insTAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622443.3:c.1147-100_1147-99insTAGG	ENSP00000482268.2:n.1147-100_1147-99insTAGG
ENST00000532059.6:c.1150-100_1150-99insTAGG MANE Select	ENSP00000435712.1:n.1150-100_1150-99insTAGG
ENST00000335135.8:c.1147-100_1147-99insTAGG	ENSP00000334458.4:n.1147-100_1147-99insTAGG
ENST00000526021.1:n.592-100_592-99insTAGG
ENST00000528712.5:c.529-100_529-99insTAGG	ENSP00000435043.1:n.529-100_529-99insTAGG
ENST00000532059.5:c.1150-100_1150-99insTAGG	ENSP00000435712.1:n.1150-100_1150-99insTAGG
ENST00000622443.2:c.1144-100_1144-99insTAGG	ENSP00000482268.1:n.1144-100_1144-99insTAGG
NM_001308093.1:c.1150-100_1150-99insTAGG	NP_001295022.1:n.1150-100_1150-99insTAGG
NM_001308094.1:c.529-100_529-99insTAGG	NP_001295023.1:n.529-100_529-99insTAGG
NM_002052.3:c.1147-100_1147-99insTAGG	NP_002043.2:n.1147-100_1147-99insTAGG
NM_002052.4:c.1147-100_1147-99insTAGG	NP_002043.2:n.1147-100_1147-99insTAGG
XM_005272385.3:c.1150-100_1150-99insTAGG	XP_005272442.1:n.1150-100_1150-99insTAGG
XM_005272386.1:c.1150-100_1150-99insTAGG	XP_005272443.1:n.1150-100_1150-99insTAGG
XM_006716248.1:c.1150-100_1150-99insTAGG	XP_006716311.1:n.1150-100_1150-99insTAGG
XM_011543817.1:c.1150-100_1150-99insTAGG	XP_011542119.1:n.1150-100_1150-99insTAGG
XM_011543818.1:c.1150-100_1150-99insTAGG	XP_011542120.1:n.1150-100_1150-99insTAGG
XM_005272385.4:c.1150-100_1150-99insTAGG	XP_005272442.1:n.1150-100_1150-99insTAGG
XM_011543817.3:c.1150-100_1150-99insTAGG	XP_011542119.1:n.1150-100_1150-99insTAGG
XM_011543818.2:c.1150-100_1150-99insTAGG	XP_011542120.1:n.1150-100_1150-99insTAGG
XM_017013312.2:c.1150-100_1150-99insTAGG	XP_016868801.1:n.1150-100_1150-99insTAGG
NM_001308093.3:c.1150-100_1150-99insTAGG MANE Select	NP_001295022.1:n.1150-100_1150-99insTAGG
NM_001308094.2:c.529-100_529-99insTAGG	NP_001295023.1:n.529-100_529-99insTAGG
NM_001374273.1:c.529-100_529-99insTAGG	NP_001361202.1:n.529-100_529-99insTAGG
NM_001374274.1:c.403-100_403-99insTAGG	NP_001361203.1:n.403-100_403-99insTAGG
NM_002052.5:c.1147-100_1147-99insTAGG	NP_002043.2:n.1147-100_1147-99insTAGG