Canonical Allele Identifier: CA14273354
Gene: ZFPM1 HGNC NCBI

Linked Data

dbSNP Id: rs55637647

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88482856C>G , CM000678.2:g.88482856C>G GRCh38
NC_000016.9:g.88549264C>G , CM000678.1:g.88549264C>G GRCh37
NC_000016.8:g.87076765C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000319555.8:c.41-3083C>G MANE Select ENSP00000326630.2:n.41-3083C>G
ENST00000319555.7:c.41-3083C>G ENSP00000326630.2:n.41-3083C>G
ENST00000562417.1:n.74-3083C>G
ENST00000562437.2:c.41-3083C>G ENSP00000480412.1:n.41-3083C>G
ENST00000563351.5:c.41-3083C>G ENSP00000484216.1:n.41-3083C>G
ENST00000569086.5:c.41-3083C>G ENSP00000482796.1:n.41-3083C>G
NM_153813.2:c.41-3083C>G NP_722520.2:n.41-3083C>G
XM_011522914.1:c.140-3083C>G XP_011521216.1:n.140-3083C>G
XM_011522916.1:c.88-3083C>G XP_011521218.1:n.88-3083C>G
XM_011522918.1:c.-14-3083C>G XP_011521220.1:n.-14-3083C>G
XM_011522912.2:c.-2331C>G XP_011521214.1:n.-2331C>G
XM_011522914.2:c.140-3083C>G XP_011521216.1:n.140-3083C>G
NM_153813.3:c.41-3083C>G MANE Select NP_722520.2:n.41-3083C>G