Canonical Allele Identifier: CA360929532

Gene: AFF4

Linked Data

• MyVariant Identifiers: chr5:g.132228084C>A (hg19) ; chr5:g.132892392C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132892392C>A , CM000667.2:g.132892392C>A	GRCh38
NC_000005.9:g.132228084C>A , CM000667.1:g.132228084C>A	GRCh37
NC_000005.8:g.132255983C>A	NCBI36
NG_030340.1:g.76271G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.2409G>T MANE Select	ENSP00000265343.5:p.Gln803His
ENST00000265343.9:c.2409G>T	ENSP00000265343.5:p.Gln803His
ENST00000378595.7:c.2409G>T	ENSP00000367858.3:p.Gln803His
NM_014423.3:c.2409G>T	NP_055238.1:p.Gln803His
XM_005271963.3:c.2409G>T	XP_005272020.1:p.Gln803His
XM_005271964.3:c.1275G>T	XP_005272021.1:p.Gln425His
XM_006714587.2:c.2322G>T	XP_006714650.1:p.Gln774His
XM_005271963.5:c.2409G>T	XP_005272020.1:p.Gln803His
XM_005271964.4:c.1275G>T	XP_005272021.1:p.Gln425His
XM_006714587.4:c.2322G>T	XP_006714650.1:p.Gln774His
NM_014423.4:c.2409G>T MANE Select	NP_055238.1:p.Gln803His