Canonical Allele Identifier: CA6027586
Community Standard Title: NM_207341.4(ZP1):c.1378G>A (p.Ala460Thr)
Gene: ZP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.60873512G>A , CM000673.2:g.60873512G>A GRCh38
NC_000011.9:g.60640985G>A , CM000673.1:g.60640985G>A GRCh37
NC_000011.8:g.60397561G>A NCBI36
NG_034138.1:g.10971G>A

Transcript Alleles

HGVS Amino-acid Change
NM_207341.4:c.1378G>A MANE Select NP_997224.2:p.Ala460Thr
ENST00000278853.10:c.1378G>A MANE Select ENSP00000278853.5:p.Ala460Thr
NM_001391943.1:c.499G>A NP_001378872.1:p.Ala167Thr
NM_001391944.1:c.184G>A NP_001378873.1:p.Ala62Thr
NM_207341.3:c.1378G>A NP_997224.2:p.Ala460Thr
ENST00000278853.9:c.1378G>A ENSP00000278853.5:p.Ala460Thr
ENST00000537203.5:n.997G>A
ENST00000543020.1:n.303G>A
ENST00000620319.1:c.499G>A ENSP00000480463.1:p.Ala167Thr
XM_011544852.1:c.499G>A XP_011543154.1:p.Ala167Thr
XM_011544852.2:c.499G>A XP_011543154.1:p.Ala167Thr
XM_011544853.1:c.499G>A XP_011543155.1:p.Ala167Thr
XM_011544853.2:c.499G>A XP_011543155.1:p.Ala167Thr