Canonical Allele Identifier: CA129878
Gene: SRP72 HGNC NCBI

Linked Data

dbSNP Id: rs587776907

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.56484842_56484843del , CM000666.2:g.56484842_56484843del GRCh38
NC_000004.11:g.57351008_57351009del , CM000666.1:g.57351008_57351009del GRCh37
NC_000004.10:g.57045765_57045766del NCBI36
NG_032796.1:g.22247_22248del

Transcript Alleles

HGVS Amino-acid change
ENST00000505314.2:c.832_833del
ENST00000510663.6:c.881_882del ENSP00000424576.1:p.Thr294LysfsTer19
ENST00000642900.1:c.1064_1065del MANE Select ENSP00000495128.1:p.Thr355LysfsTer19
ENST00000342756.9:c.1064_1065del ENSP00000342181.5:p.Thr355LysfsTer19
ENST00000505314.1:c.498_499del
ENST00000510663.5:c.881_882del ENSP00000424576.1:p.Thr294LysfsTer19
NM_001267722.1:c.881_882del NP_001254651.1:p.Thr294LysfsTer19
NM_006947.3:c.1064_1065del NP_008878.3:p.Thr355LysfsTer19
XM_005265765.3:c.1064_1065del XP_005265822.2:p.Thr355LysfsTer19
NM_006947.4:c.1064_1065del MANE Select NP_008878.3:p.Thr355LysfsTer19
NR_151856.1:n.1104_1105del
XM_024454192.1:c.1064_1065del XP_024309960.1:p.Thr355LysfsTer19
NM_001267722.2:c.881_882del NP_001254651.1:p.Thr294LysfsTer19
NR_151856.2:n.1083_1084del