Canonical Allele Identifier: CA14273374

Gene: ZFPM1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88502423T>G , CM000678.2:g.88502423T>G	GRCh38
NC_000016.9:g.88568831T>G , CM000678.1:g.88568831T>G	GRCh37
NC_000016.8:g.87096332T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319555.8:c.269-11964T>G MANE Select	ENSP00000326630.2:n.269-11964T>G
ENST00000319555.7:c.269-11964T>G	ENSP00000326630.2:n.269-11964T>G
ENST00000562437.2:c.269-11964T>G	ENSP00000480412.1:n.269-11964T>G
ENST00000563351.5:c.146-11964T>G	ENSP00000484216.1:n.146-11964T>G
ENST00000569086.5:c.269-11964T>G	ENSP00000482796.1:n.269-11964T>G
NM_153813.2:c.269-11964T>G	NP_722520.2:n.269-11964T>G
XM_011522912.1:c.407-11964T>G	XP_011521214.1:n.407-11964T>G
XM_011522913.1:c.516+13270T>G	XP_011521215.1:n.516+13270T>G
XM_011522914.1:c.368-11964T>G	XP_011521216.1:n.368-11964T>G
XM_011522915.1:c.233-11964T>G	XP_011521217.1:n.233-11964T>G
XM_011522916.1:c.315+13270T>G	XP_011521218.1:n.315+13270T>G
XM_011522918.1:c.215-11964T>G	XP_011521220.1:n.215-11964T>G
XM_011522912.2:c.407-11964T>G	XP_011521214.1:n.407-11964T>G
XM_011522914.2:c.368-11964T>G	XP_011521216.1:n.368-11964T>G
XM_017022982.1:c.7+11949T>G	XP_016878471.1:n.7+11949T>G
NM_153813.3:c.269-11964T>G MANE Select	NP_722520.2:n.269-11964T>G