Canonical Allele Identifier: CA14234675

Gene: ZFPM1

Linked Data

• dbSNP Id: rs904790
• gnomAD v2: 16-88528780-T-C
• gnomAD v3: 16-88462372-T-C
• gnomAD v4: 16-88462372-T-C
• MyVariant Identifiers: chr16:g.88528780T>C (hg19) ; chr16:g.88462372T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88462372T>C , CM000678.2:g.88462372T>C	GRCh38
NC_000016.9:g.88528780T>C , CM000678.1:g.88528780T>C	GRCh37
NC_000016.8:g.87056281T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000319555.8:c.40+8694T>C MANE Select	ENSP00000326630.2:n.40+8694T>C
ENST00000319555.7:c.40+8694T>C	ENSP00000326630.2:n.40+8694T>C
ENST00000562417.1:n.73+8694T>C
ENST00000562437.2:c.40+8694T>C	ENSP00000480412.1:n.40+8694T>C
ENST00000563351.5:c.40+8694T>C	ENSP00000484216.1:n.40+8694T>C
ENST00000569086.5:c.40+8694T>C	ENSP00000482796.1:n.40+8694T>C
NM_153813.2:c.40+8694T>C	NP_722520.2:n.40+8694T>C
XM_011522914.1:c.139+10434T>C	XP_011521216.1:n.139+10434T>C
XM_011522916.1:c.87+10434T>C	XP_011521218.1:n.87+10434T>C
XM_011522918.1:c.-15+10743T>C	XP_011521220.1:n.-15+10743T>C
XM_011522914.2:c.139+10434T>C	XP_011521216.1:n.139+10434T>C
NM_153813.3:c.40+8694T>C MANE Select	NP_722520.2:n.40+8694T>C