Canonical Allele Identifier: CA461770884

Gene: ZFHX4

Linked Data

• dbSNP Id: rs1338716606
• gnomAD v2: 8-77776576-T-A
• gnomAD v3: 8-76864340-T-A
• gnomAD v4: 8-76864340-T-A
• MyVariant Identifiers: chr8:g.77776576T>A (hg19) ; chr8:g.76864340T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864340T>A , CM000670.2:g.76864340T>A	GRCh38
NC_000008.10:g.77776576T>A , CM000670.1:g.77776576T>A	GRCh37
NC_000008.9:g.77939131T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10626T>A MANE Select	ENSP00000498627.1:p.Pro3542=
ENST00000518282.5:c.10548T>A	ENSP00000430848.1:p.Pro3516=
ENST00000521891.6:c.10626T>A	ENSP00000430497.2:p.Pro3542=
NM_024721.4:c.10626T>A	NP_078997.4:p.Pro3542=
XM_011517592.1:c.10626T>A	XP_011515894.1:p.Pro3542=
XM_011517593.1:c.10626T>A	XP_011515895.1:p.Pro3542=
XM_011517594.1:c.10626T>A	XP_011515896.1:p.Pro3542=
XM_011517595.1:c.10626T>A	XP_011515897.1:p.Pro3542=
XM_011517596.1:c.10548T>A	XP_011515898.1:p.Pro3516=
XM_011517597.1:c.10509T>A	XP_011515899.1:p.Pro3503=
XM_011517592.3:c.10626T>A	XP_011515894.1:p.Pro3542=
XM_011517593.2:c.10626T>A	XP_011515895.1:p.Pro3542=
XM_011517594.2:c.10626T>A	XP_011515896.1:p.Pro3542=
XM_011517595.2:c.10626T>A	XP_011515897.1:p.Pro3542=
XM_011517596.2:c.10548T>A	XP_011515898.1:p.Pro3516=
XM_011517597.2:c.10509T>A	XP_011515899.1:p.Pro3503=
XM_017013845.1:c.10431T>A	XP_016869334.1:p.Pro3477=
NM_024721.5:c.10626T>A MANE Select	NP_078997.4:p.Pro3542=