Canonical Allele Identifier: CA4788580
Gene: ZFHX4 HGNC NCBI

Linked Data

dbSNP Id: rs376991694
gnomAD v2: 8-77776608-C-T
gnomAD v3: 8-76864372-C-T
gnomAD v4: 8-76864372-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.76864372C>T , CM000670.2:g.76864372C>T GRCh38
NC_000008.10:g.77776608C>T , CM000670.1:g.77776608C>T GRCh37
NC_000008.9:g.77939163C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651372.2:c.10658C>T MANE Select ENSP00000498627.1:p.Thr3553Met
ENST00000518282.5:c.10580C>T ENSP00000430848.1:p.Thr3527Met
ENST00000521891.6:c.10658C>T ENSP00000430497.2:p.Thr3553Met
NM_024721.4:c.10658C>T NP_078997.4:p.Thr3553Met
XM_011517592.1:c.10658C>T XP_011515894.1:p.Thr3553Met
XM_011517593.1:c.10658C>T XP_011515895.1:p.Thr3553Met
XM_011517594.1:c.10658C>T XP_011515896.1:p.Thr3553Met
XM_011517595.1:c.10658C>T XP_011515897.1:p.Thr3553Met
XM_011517596.1:c.10580C>T XP_011515898.1:p.Thr3527Met
XM_011517597.1:c.10541C>T XP_011515899.1:p.Thr3514Met
XM_011517592.3:c.10658C>T XP_011515894.1:p.Thr3553Met
XM_011517593.2:c.10658C>T XP_011515895.1:p.Thr3553Met
XM_011517594.2:c.10658C>T XP_011515896.1:p.Thr3553Met
XM_011517595.2:c.10658C>T XP_011515897.1:p.Thr3553Met
XM_011517596.2:c.10580C>T XP_011515898.1:p.Thr3527Met
XM_011517597.2:c.10541C>T XP_011515899.1:p.Thr3514Met
XM_017013845.1:c.10463C>T XP_016869334.1:p.Thr3488Met
NM_024721.5:c.10658C>T MANE Select NP_078997.4:p.Thr3553Met