Canonical Allele Identifier: CA360928121

Gene: AFF4

Linked Data

• MyVariant Identifiers: chr5:g.132227820A>C (hg19) ; chr5:g.132892128A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132892128A>C , CM000667.2:g.132892128A>C	GRCh38
NC_000005.9:g.132227820A>C , CM000667.1:g.132227820A>C	GRCh37
NC_000005.8:g.132255719A>C	NCBI36
NG_030340.1:g.76535T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.2637+36T>G MANE Select	ENSP00000265343.5:n.2637+36T>G
ENST00000265343.9:c.2637+36T>G	ENSP00000265343.5:n.2637+36T>G
ENST00000378595.7:c.2673T>G	ENSP00000367858.3:p.His891Gln
NM_014423.3:c.2637+36T>G	NP_055238.1:n.2637+36T>G
XM_005271963.3:c.2637+36T>G	XP_005272020.1:n.2637+36T>G
XM_005271964.3:c.1503+36T>G	XP_005272021.1:n.1503+36T>G
XM_006714587.2:c.2550+36T>G	XP_006714650.1:n.2550+36T>G
XM_005271963.5:c.2637+36T>G	XP_005272020.1:n.2637+36T>G
XM_005271964.4:c.1503+36T>G	XP_005272021.1:n.1503+36T>G
XM_006714587.4:c.2550+36T>G	XP_006714650.1:n.2550+36T>G
NM_014423.4:c.2637+36T>G MANE Select	NP_055238.1:n.2637+36T>G