Canonical Allele Identifier: CA356995781
Gene: SRP72 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.56469676G>C , CM000666.2:g.56469676G>C GRCh38
NC_000004.11:g.57335842G>C , CM000666.1:g.57335842G>C GRCh37
NC_000004.10:g.57030599G>C NCBI36
NG_032796.1:g.7081G>C

Transcript Alleles

HGVS Amino-acid Change
NM_006947.4:c.133G>C MANE Select NP_008878.3:p.Val45Leu
ENST00000642900.1:c.133G>C MANE Select ENSP00000495128.1:p.Val45Leu
NM_001267722.1:c.133G>C NP_001254651.1:p.Val45Leu
NM_001267722.2:c.133G>C NP_001254651.1:p.Val45Leu
NM_006947.3:c.133G>C NP_008878.3:p.Val45Leu
NR_151856.1:n.173G>C
NR_151856.2:n.152G>C
ENST00000342756.9:c.133G>C ENSP00000342181.5:p.Val45Leu
ENST00000504757.2:c.133G>C ENSP00000473576.1:p.Val45Leu
ENST00000505314.2:c.33G>C
ENST00000510663.5:c.133G>C ENSP00000424576.1:p.Val45Leu
ENST00000510663.6:c.133G>C ENSP00000424576.1:p.Val45Leu
XM_005265765.3:c.133G>C XP_005265822.2:p.Val45Leu
XM_024454192.1:c.133G>C XP_024309960.1:p.Val45Leu