Canonical Allele Identifier: CA2581389472
Community Standard Title: NM_022142.5(ELSPBP1):c.*8-627C>G
Gene: ELSPBP1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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