Canonical Allele Identifier: CA2339699219
Gene: ELSPBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48024211C= , CM000681.2:g.48024211C= GRCh38
NC_000019.9:g.48527468C= , CM000681.1:g.48527468C= GRCh37
NC_000019.8:g.53219280C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339841.7:c.*8-741C= MANE Select ENSP00000340660.2:n.*8-741C=
ENST00000339841.6:c.*8-741C= ENSP00000340660.2:n.*8-741C=
ENST00000593413.1:c.239-720C= ENSP00000470551.1:n.239-720C=
ENST00000593782.1:c.514-741C=
ENST00000597519.5:c.*8-741C= ENSP00000471690.1:n.*8-741C=
ENST00000619003.4:c.*13-741C= ENSP00000481506.1:n.*13-741C=
NM_022142.4:c.*8-741C= NP_071425.3:n.*8-741C=
XM_006723322.2:c.*8-741C= XP_006723385.1:n.*8-741C=
XM_017027130.1:c.*8-741C= XP_016882619.1:n.*8-741C=
NM_022142.5:c.*8-741C= MANE Select NP_071425.3:n.*8-741C=