Canonical Allele Identifier: CA446498848

Gene: AFF4

Linked Data

• MyVariant Identifiers: chr5:g.132227907T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132892215T>A , CM000667.2:g.132892215T>A	GRCh38
NC_000005.9:g.132227907T>A , CM000667.1:g.132227907T>A	GRCh37
NC_000005.8:g.132255806T>A	NCBI36
NG_030340.1:g.76448A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265343.10:c.2586A>T MANE Select	ENSP00000265343.5:p.Ser862=
ENST00000265343.9:c.2586A>T	ENSP00000265343.5:p.Ser862=
ENST00000378595.7:c.2586A>T	ENSP00000367858.3:p.Ser862=
NM_014423.3:c.2586A>T	NP_055238.1:p.Ser862=
XM_005271963.3:c.2586A>T	XP_005272020.1:p.Ser862=
XM_005271964.3:c.1452A>T	XP_005272021.1:p.Ser484=
XM_006714587.2:c.2499A>T	XP_006714650.1:p.Ser833=
XM_005271963.5:c.2586A>T	XP_005272020.1:p.Ser862=
XM_005271964.4:c.1452A>T	XP_005272021.1:p.Ser484=
XM_006714587.4:c.2499A>T	XP_006714650.1:p.Ser833=
NM_014423.4:c.2586A>T MANE Select	NP_055238.1:p.Ser862=