Canonical Allele Identifier: CA4788574

Gene: ZFHX4

Linked Data

• dbSNP Id: rs772214396
• ExAC: 8:77776580 TCTC / T
• gnomAD v2: 8-77776580-TCTC-T
• gnomAD v3: 8-76864344-TCTC-T
• gnomAD v4: 8-76864344-TCTC-T
• MyVariant Identifiers: chr8:g.77776581_77776583del (hg19) ; chr8:g.76864345_76864347del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864350_76864352del , CM000670.2:g.76864350_76864352del	GRCh38
NC_000008.10:g.77776586_77776588del , CM000670.1:g.77776586_77776588del	GRCh37
NC_000008.9:g.77939141_77939143del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10636_10638del MANE Select	ENSP00000498627.1:p.Pro3546del
ENST00000518282.5:c.10558_10560del	ENSP00000430848.1:p.Pro3520del
ENST00000521891.6:c.10636_10638del	ENSP00000430497.2:p.Pro3546del
NM_024721.4:c.10636_10638del	NP_078997.4:p.Pro3546del
XM_011517592.1:c.10636_10638del	XP_011515894.1:p.Pro3546del
XM_011517593.1:c.10636_10638del	XP_011515895.1:p.Pro3546del
XM_011517594.1:c.10636_10638del	XP_011515896.1:p.Pro3546del
XM_011517595.1:c.10636_10638del	XP_011515897.1:p.Pro3546del
XM_011517596.1:c.10558_10560del	XP_011515898.1:p.Pro3520del
XM_011517597.1:c.10519_10521del	XP_011515899.1:p.Pro3507del
XM_011517592.3:c.10636_10638del	XP_011515894.1:p.Pro3546del
XM_011517593.2:c.10636_10638del	XP_011515895.1:p.Pro3546del
XM_011517594.2:c.10636_10638del	XP_011515896.1:p.Pro3546del
XM_011517595.2:c.10636_10638del	XP_011515897.1:p.Pro3546del
XM_011517596.2:c.10558_10560del	XP_011515898.1:p.Pro3520del
XM_011517597.2:c.10519_10521del	XP_011515899.1:p.Pro3507del
XM_017013845.1:c.10441_10443del	XP_016869334.1:p.Pro3481del
NM_024721.5:c.10636_10638del MANE Select	NP_078997.4:p.Pro3546del