Canonical Allele Identifier: CA397055978

Gene: ZFPM1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88534333A>C , CM000678.2:g.88534333A>C	GRCh38
NC_000016.9:g.88600741A>C , CM000678.1:g.88600741A>C	GRCh37
NC_000016.8:g.87128242A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_153813.3:c.2375A>C MANE Select	NP_722520.2:p.Asp792Ala
ENST00000319555.8:c.2375A>C MANE Select	ENSP00000326630.2:p.Asp792Ala
NM_153813.2:c.2375A>C	NP_722520.2:p.Asp792Ala
ENST00000319555.7:c.2375A>C	ENSP00000326630.2:p.Asp792Ala
XM_011522912.1:c.2513A>C	XP_011521214.1:p.Asp838Ala
XM_011522912.2:c.2513A>C	XP_011521214.1:p.Asp838Ala
XM_011522913.1:c.2489A>C	XP_011521215.1:p.Asp830Ala
XM_011522914.1:c.2474A>C	XP_011521216.1:p.Asp825Ala
XM_011522914.2:c.2474A>C	XP_011521216.1:p.Asp825Ala
XM_011522915.1:c.2339A>C	XP_011521217.1:p.Asp780Ala
XM_011522916.1:c.2288A>C	XP_011521218.1:p.Asp763Ala
XM_011522917.1:c.2195A>C	XP_011521219.1:p.Asp732Ala
XM_011522917.2:c.2195A>C	XP_011521219.1:p.Asp732Ala
XM_011522918.1:c.2321A>C	XP_011521220.1:p.Asp774Ala
XM_017022982.1:c.2114A>C	XP_016878471.1:p.Asp705Ala