Canonical Allele Identifier: CA807697963

Gene: NKX2-5

Linked Data

• dbSNP Id: rs767484865
• MyVariant Identifiers: chr5:g.172662115G>C (hg19) ; chr5:g.173235112G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173235112G>C , CM000667.2:g.173235112G>C	GRCh38
NC_000005.9:g.172662115G>C , CM000667.1:g.172662115G>C	GRCh37
NC_000005.8:g.172594721G>C	NCBI36
NG_013340.1:g.5201C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.-29C>G MANE Select	ENSP00000327758.4:n.-29C>G
ENST00000329198.4:c.-29C>G	ENSP00000327758.4:n.-29C>G
ENST00000424406.2:c.-29C>G	ENSP00000395378.2:n.-29C>G
ENST00000517440.1:c.-29C>G	ENSP00000429905.1:n.-29C>G
ENST00000521848.1:c.-29C>G	ENSP00000427906.1:n.-29C>G
NM_001166175.1:c.-29C>G	NP_001159647.1:n.-29C>G
NM_001166176.1:c.-29C>G	NP_001159648.1:n.-29C>G
NM_004387.3:c.-29C>G	NP_004378.1:n.-29C>G
XM_017009071.2:c.-29C>G	XP_016864560.1:n.-29C>G
NM_004387.4:c.-29C>G MANE Select	NP_004378.1:n.-29C>G
NM_001166175.2:c.-29C>G	NP_001159647.1:n.-29C>G
NM_001166176.2:c.-29C>G	NP_001159648.1:n.-29C>G