Canonical Allele Identifier: CA2581389473
Community Standard Title: NM_022142.5(ELSPBP1):c.*8-627C>A
Gene: ELSPBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48024325C>A , CM000681.2:g.48024325C>A GRCh38
NC_000019.9:g.48527582C>A , CM000681.1:g.48527582C>A GRCh37
NC_000019.8:g.53219394C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_022142.5:c.*8-627C>A MANE Select NP_071425.3:n.*8-627C>A
ENST00000339841.7:c.*8-627C>A MANE Select ENSP00000340660.2:n.*8-627C>A
NM_022142.4:c.*8-627C>A NP_071425.3:n.*8-627C>A
ENST00000339841.6:c.*8-627C>A ENSP00000340660.2:n.*8-627C>A
ENST00000593413.1:c.239-606C>A ENSP00000470551.1:n.239-606C>A
ENST00000593782.1:c.514-627C>A
ENST00000597519.5:c.*8-627C>A ENSP00000471690.1:n.*8-627C>A
ENST00000619003.4:c.*13-627C>A ENSP00000481506.1:n.*13-627C>A
XM_006723322.2:c.*8-627C>A XP_006723385.1:n.*8-627C>A
XM_017027130.1:c.*8-627C>A XP_016882619.1:n.*8-627C>A