Canonical Allele Identifier: CA1764080590

Gene: GATA4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11749782_11749785delinsTCTC , CM000670.2:g.11749782_11749785delinsTCTC	GRCh38
NC_000008.10:g.11607291_11607294delinsTCTC , CM000670.1:g.11607291_11607294delinsTCTC	GRCh37
NC_000008.9:g.11644700_11644703delinsTCTC	NCBI36
NG_008177.2:g.77864_77867delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622443.3:c.784-329_784-326delinsTCTC	ENSP00000482268.2:n.784-329_784-326delinsTCTC
ENST00000532059.6:c.787-329_787-326delinsTCTC MANE Select	ENSP00000435712.1:n.787-329_787-326delinsTCTC
ENST00000335135.8:c.784-329_784-326delinsTCTC	ENSP00000334458.4:n.784-329_784-326delinsTCTC
ENST00000526716.5:c.166-329_166-326delinsTCTC	ENSP00000435347.1:n.166-329_166-326delinsTCTC
ENST00000528712.5:c.166-329_166-326delinsTCTC	ENSP00000435043.1:n.166-329_166-326delinsTCTC
ENST00000532059.5:c.787-329_787-326delinsTCTC	ENSP00000435712.1:n.787-329_787-326delinsTCTC
ENST00000622443.2:c.781-329_781-326delinsTCTC	ENSP00000482268.1:n.781-329_781-326delinsTCTC
NM_001308093.1:c.787-329_787-326delinsTCTC	NP_001295022.1:n.787-329_787-326delinsTCTC
NM_001308094.1:c.166-329_166-326delinsTCTC	NP_001295023.1:n.166-329_166-326delinsTCTC
NM_002052.3:c.784-329_784-326delinsTCTC	NP_002043.2:n.784-329_784-326delinsTCTC
NM_002052.4:c.784-329_784-326delinsTCTC	NP_002043.2:n.784-329_784-326delinsTCTC
XM_005272385.3:c.787-329_787-326delinsTCTC	XP_005272442.1:n.787-329_787-326delinsTCTC
XM_005272386.1:c.787-329_787-326delinsTCTC	XP_005272443.1:n.787-329_787-326delinsTCTC
XM_006716248.1:c.787-329_787-326delinsTCTC	XP_006716311.1:n.787-329_787-326delinsTCTC
XM_011543817.1:c.787-329_787-326delinsTCTC	XP_011542119.1:n.787-329_787-326delinsTCTC
XM_011543818.1:c.787-329_787-326delinsTCTC	XP_011542120.1:n.787-329_787-326delinsTCTC
XM_005272385.4:c.787-329_787-326delinsTCTC	XP_005272442.1:n.787-329_787-326delinsTCTC
XM_011543817.3:c.787-329_787-326delinsTCTC	XP_011542119.1:n.787-329_787-326delinsTCTC
XM_011543818.2:c.787-329_787-326delinsTCTC	XP_011542120.1:n.787-329_787-326delinsTCTC
XM_017013312.2:c.787-329_787-326delinsTCTC	XP_016868801.1:n.787-329_787-326delinsTCTC
NM_001308093.3:c.787-329_787-326delinsTCTC MANE Select	NP_001295022.1:n.787-329_787-326delinsTCTC
NM_001308094.2:c.166-329_166-326delinsTCTC	NP_001295023.1:n.166-329_166-326delinsTCTC
NM_001374273.1:c.166-329_166-326delinsTCTC	NP_001361202.1:n.166-329_166-326delinsTCTC
NM_001374274.1:c.165+697_165+700delinsTCTC	NP_001361203.1:n.165+697_165+700delinsTCTC
NM_002052.5:c.784-329_784-326delinsTCTC	NP_002043.2:n.784-329_784-326delinsTCTC