Canonical Allele Identifier: CA3122577602
Community Standard Title: NM_006947.4(SRP72):c.826-39T=
Gene: SRP72 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.56483100T= , CM000666.2:g.56483100T= GRCh38
NC_000004.11:g.57349266T= , CM000666.1:g.57349266T= GRCh37
NC_000004.10:g.57044023T= NCBI36
NG_032796.1:g.20505T=

Transcript Alleles

HGVS Amino-acid Change
NM_006947.4:c.826-39T= MANE Select NP_008878.3:n.826-39T=
ENST00000642900.1:c.826-39T= MANE Select ENSP00000495128.1:n.826-39T=
NM_001267722.1:c.643-39T= NP_001254651.1:n.643-39T=
NM_001267722.2:c.643-39T= NP_001254651.1:n.643-39T=
NM_006947.3:c.826-39T= NP_008878.3:n.826-39T=
NR_151856.1:n.866-39T=
NR_151856.2:n.845-39T=
ENST00000342756.9:c.826-39T= ENSP00000342181.5:n.826-39T=
ENST00000505314.1:c.392-1636T=
ENST00000505314.2:c.726-1636T=
ENST00000510663.5:c.643-39T= ENSP00000424576.1:n.643-39T=
ENST00000510663.6:c.643-39T= ENSP00000424576.1:n.643-39T=
XM_005265765.3:c.826-39T= XP_005265822.2:n.826-39T=
XM_024454192.1:c.826-39T= XP_024309960.1:n.826-39T=