Canonical Allele Identifier: CA807697008

Gene: NKX2-5

Linked Data

• dbSNP Id: rs1450204897
• gnomAD v3: 5-173234575-CGATTGGA-C
• gnomAD v4: 5-173234575-CGATTGGA-C
• MyVariant Identifiers: chr5:g.172661579_172661585del (hg19) ; chr5:g.173234576_173234582del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173234576_173234582del , CM000667.2:g.173234576_173234582del	GRCh38
NC_000005.9:g.172661579_172661585del , CM000667.1:g.172661579_172661585del	GRCh37
NC_000005.8:g.172594185_172594191del	NCBI36
NG_013340.1:g.5731_5737del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.334+168_334+174del MANE Select	ENSP00000327758.4:n.334+168_334+174del
ENST00000329198.4:c.334+168_334+174del	ENSP00000327758.4:n.334+168_334+174del
ENST00000424406.2:c.334+168_334+174del	ENSP00000395378.2:n.334+168_334+174del
ENST00000517440.1:c.334+168_334+174del	ENSP00000429905.1:n.334+168_334+174del
ENST00000521848.1:c.334+168_334+174del	ENSP00000427906.1:n.334+168_334+174del
NM_001166175.1:c.334+168_334+174del	NP_001159647.1:n.334+168_334+174del
NM_001166176.1:c.334+168_334+174del	NP_001159648.1:n.334+168_334+174del
NM_004387.3:c.334+168_334+174del	NP_004378.1:n.334+168_334+174del
XM_017009071.2:c.334+168_334+174del	XP_016864560.1:n.334+168_334+174del
NM_004387.4:c.334+168_334+174del MANE Select	NP_004378.1:n.334+168_334+174del
NM_001166175.2:c.334+168_334+174del	NP_001159647.1:n.334+168_334+174del
NM_001166176.2:c.334+168_334+174del	NP_001159648.1:n.334+168_334+174del