Canonical Allele Identifier: CA447974984

Gene: NKX2-5

Linked Data

• MyVariant Identifiers: chr5:g.172660172T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173233169T>G , CM000667.2:g.173233169T>G	GRCh38
NC_000005.9:g.172660172T>G , CM000667.1:g.172660172T>G	GRCh37
NC_000005.8:g.172592778T>G	NCBI36
NG_013340.1:g.7144A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.375A>C MANE Select	ENSP00000327758.4:p.Thr125=
ENST00000329198.4:c.375A>C	ENSP00000327758.4:p.Thr125=
ENST00000424406.2:c.*328A>C	ENSP00000395378.2:n.*328A>C
ENST00000521848.1:c.*174A>C	ENSP00000427906.1:n.*174A>C
NM_001166175.1:c.*328A>C	NP_001159647.1:n.*328A>C
NM_001166176.1:c.*174A>C	NP_001159648.1:n.*174A>C
NM_004387.3:c.375A>C	NP_004378.1:p.Thr125=
NM_004387.4:c.375A>C MANE Select	NP_004378.1:p.Thr125=
NM_001166175.2:c.*328A>C	NP_001159647.1:n.*328A>C
NM_001166176.2:c.*174A>C	NP_001159648.1:n.*174A>C