Canonical Allele Identifier: CA14285684
Gene: ZFHX3 HGNC NCBI
COSMIC:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73017721C>T , CM000678.2:g.73017721C>T GRCh38
NC_000016.9:g.73051620C>T , CM000678.1:g.73051620C>T GRCh37
NC_000016.8:g.71609121C>T NCBI36
NG_013211.1:g.45915G>A
NG_013211.2:g.879211G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000268489.10:c.-50+30031G>A MANE Select ENSP00000268489.5:n.-50+30031G>A
ENST00000641206.2:c.-50+40809G>A ENSP00000493252.1:n.-50+40809G>A
ENST00000268489.9:c.-50+30031G>A ENSP00000268489.5:n.-50+30031G>A
ENST00000397992.5:c.-24+40809G>A ENSP00000438926.3:n.-24+40809G>A
NM_001164766.1:c.-24+40809G>A NP_001158238.1:n.-24+40809G>A
NM_006885.3:c.-50+30031G>A NP_008816.3:n.-50+30031G>A
XM_005255957.2:c.-50+30031G>A XP_005256014.1:n.-50+30031G>A
XM_005255957.4:c.-50+30031G>A XP_005256014.1:n.-50+30031G>A
XM_017023251.2:c.70+30031G>A XP_016878740.1:n.70+30031G>A
XM_024450291.1:c.70+30031G>A XP_024306059.1:n.70+30031G>A
NM_006885.4:c.-50+30031G>A MANE Select NP_008816.3:n.-50+30031G>A
NM_001164766.2:c.-24+40809G>A NP_001158238.1:n.-24+40809G>A
NM_001386735.1:c.-49-57527G>A NP_001373664.1:n.-49-57527G>A