Canonical Allele Identifier: CA1601617112

Gene: NKX2-5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173235040_173235044delinsTTGAC , CM000667.2:g.173235040_173235044delinsTTGAC	GRCh38
NC_000005.9:g.172662043_172662047delinsTTGAC , CM000667.1:g.172662043_172662047delinsTTGAC	GRCh37
NC_000005.8:g.172594649_172594653delinsTTGAC	NCBI36
NG_013340.1:g.5269_5273delinsGTCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.40_44delinsGTCAA MANE Select	ENSP00000327758.4:p.Val14=
ENST00000329198.4:c.40_44delinsGTCAA	ENSP00000327758.4:p.Val14=
ENST00000424406.2:c.40_44delinsGTCAA	ENSP00000395378.2:p.Val14=
ENST00000517440.1:c.40_44delinsGTCAA	ENSP00000429905.1:p.Val14=
ENST00000521848.1:c.40_44delinsGTCAA	ENSP00000427906.1:p.Val14=
NM_001166175.1:c.40_44delinsGTCAA	NP_001159647.1:p.Val14=
NM_001166176.1:c.40_44delinsGTCAA	NP_001159648.1:p.Val14=
NM_004387.3:c.40_44delinsGTCAA	NP_004378.1:p.Val14=
XM_017009071.2:c.40_44delinsGTCAA	XP_016864560.1:p.Val14=
NM_004387.4:c.40_44delinsGTCAA MANE Select	NP_004378.1:p.Val14=
NM_001166175.2:c.40_44delinsGTCAA	NP_001159647.1:p.Val14=
NM_001166176.2:c.40_44delinsGTCAA	NP_001159648.1:p.Val14=