Canonical Allele Identifier: CA2676543001

Gene: NKX2-5

Linked Data

• gnomAD v4: 5-173234720-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173234720G>T , CM000667.2:g.173234720G>T	GRCh38
NC_000005.9:g.172661723G>T , CM000667.1:g.172661723G>T	GRCh37
NC_000005.8:g.172594329G>T	NCBI36
NG_013340.1:g.5593C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.334+30C>A MANE Select	ENSP00000327758.4:n.334+30C>A
ENST00000329198.4:c.334+30C>A	ENSP00000327758.4:n.334+30C>A
ENST00000424406.2:c.334+30C>A	ENSP00000395378.2:n.334+30C>A
ENST00000517440.1:c.334+30C>A	ENSP00000429905.1:n.334+30C>A
ENST00000521848.1:c.334+30C>A	ENSP00000427906.1:n.334+30C>A
NM_001166175.1:c.334+30C>A	NP_001159647.1:n.334+30C>A
NM_001166176.1:c.334+30C>A	NP_001159648.1:n.334+30C>A
NM_004387.3:c.334+30C>A	NP_004378.1:n.334+30C>A
XM_017009071.2:c.334+30C>A	XP_016864560.1:n.334+30C>A
NM_004387.4:c.334+30C>A MANE Select	NP_004378.1:n.334+30C>A
NM_001166175.2:c.334+30C>A	NP_001159647.1:n.334+30C>A
NM_001166176.2:c.334+30C>A	NP_001159648.1:n.334+30C>A