Canonical Allele Identifier: CA4788552

Gene: ZFHX4

Linked Data

• dbSNP Id: rs372791764
• ExAC: 8:77776467 A / C
• gnomAD v2: 8-77776467-A-C
• gnomAD v3: 8-76864231-A-C
• gnomAD v4: 8-76864231-A-C
• MyVariant Identifiers: chr8:g.77776467A>C (hg19) ; chr8:g.76864231A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864231A>C , CM000670.2:g.76864231A>C	GRCh38
NC_000008.10:g.77776467A>C , CM000670.1:g.77776467A>C	GRCh37
NC_000008.9:g.77939022A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10517A>C MANE Select	ENSP00000498627.1:p.Gln3506Pro
ENST00000518282.5:c.10439A>C	ENSP00000430848.1:p.Gln3480Pro
ENST00000521891.6:c.10517A>C	ENSP00000430497.2:p.Gln3506Pro
NM_024721.4:c.10517A>C	NP_078997.4:p.Gln3506Pro
XM_011517592.1:c.10517A>C	XP_011515894.1:p.Gln3506Pro
XM_011517593.1:c.10517A>C	XP_011515895.1:p.Gln3506Pro
XM_011517594.1:c.10517A>C	XP_011515896.1:p.Gln3506Pro
XM_011517595.1:c.10517A>C	XP_011515897.1:p.Gln3506Pro
XM_011517596.1:c.10439A>C	XP_011515898.1:p.Gln3480Pro
XM_011517597.1:c.10400A>C	XP_011515899.1:p.Gln3467Pro
XM_011517592.3:c.10517A>C	XP_011515894.1:p.Gln3506Pro
XM_011517593.2:c.10517A>C	XP_011515895.1:p.Gln3506Pro
XM_011517594.2:c.10517A>C	XP_011515896.1:p.Gln3506Pro
XM_011517595.2:c.10517A>C	XP_011515897.1:p.Gln3506Pro
XM_011517596.2:c.10439A>C	XP_011515898.1:p.Gln3480Pro
XM_011517597.2:c.10400A>C	XP_011515899.1:p.Gln3467Pro
XM_017013845.1:c.10322A>C	XP_016869334.1:p.Gln3441Pro
NM_024721.5:c.10517A>C MANE Select	NP_078997.4:p.Gln3506Pro