Canonical Allele Identifier: CA723625070

Gene: ZFHX3

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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