Canonical Allele Identifier: CA1601616918

Gene: NKX2-5

Linked Data

• dbSNP Id: rs1761425658

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173234671_173234673del , CM000667.2:g.173234671_173234673del	GRCh38
NC_000005.9:g.172661674_172661676del , CM000667.1:g.172661674_172661676del	GRCh37
NC_000005.8:g.172594280_172594282del	NCBI36
NG_013340.1:g.5640_5642del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.334+77_334+79del MANE Select	ENSP00000327758.4:n.334+77_334+79del
ENST00000329198.4:c.334+77_334+79del	ENSP00000327758.4:n.334+77_334+79del
ENST00000424406.2:c.334+77_334+79del	ENSP00000395378.2:n.334+77_334+79del
ENST00000517440.1:c.334+77_334+79del	ENSP00000429905.1:n.334+77_334+79del
ENST00000521848.1:c.334+77_334+79del	ENSP00000427906.1:n.334+77_334+79del
NM_001166175.1:c.334+77_334+79del	NP_001159647.1:n.334+77_334+79del
NM_001166176.1:c.334+77_334+79del	NP_001159648.1:n.334+77_334+79del
NM_004387.3:c.334+77_334+79del	NP_004378.1:n.334+77_334+79del
XM_017009071.2:c.334+77_334+79del	XP_016864560.1:n.334+77_334+79del
NM_004387.4:c.334+77_334+79del MANE Select	NP_004378.1:n.334+77_334+79del
NM_001166175.2:c.334+77_334+79del	NP_001159647.1:n.334+77_334+79del
NM_001166176.2:c.334+77_334+79del	NP_001159648.1:n.334+77_334+79del