Canonical Allele Identifier: CA733451164
Gene: SRSF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23974359T>G , CM000663.2:g.23974359T>G GRCh38
NC_000001.10:g.24300849T>G , CM000663.1:g.24300849T>G GRCh37
NC_000001.9:g.24173436T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000492112.3:c.274+615A>C MANE Select ENSP00000420195.1:n.274+615A>C
ENST00000338597.9:n.134+615A>C
ENST00000341154.10:n.1343+615A>C
ENST00000343255.9:c.274+615A>C ENSP00000344149.4:n.274+615A>C
ENST00000344989.10:c.274+615A>C ENSP00000342913.5:n.274+615A>C
ENST00000374452.9:c.274+615A>C ENSP00000363576.5:n.274+615A>C
ENST00000374453.7:c.274+615A>C ENSP00000363577.3:n.274+615A>C
ENST00000453840.7:c.274+615A>C ENSP00000388991.3:n.274+615A>C
ENST00000473754.1:n.79+615A>C
ENST00000473858.5:c.66-2347A>C ENSP00000473293.1:n.66-2347A>C
ENST00000484146.6:c.274+615A>C ENSP00000419813.2:n.274+615A>C
ENST00000485841.5:n.2679+615A>C
ENST00000492112.2:c.274+615A>C ENSP00000420195.1:n.274+615A>C
ENST00000495785.1:c.*490+615A>C ENSP00000473291.1:n.*490+615A>C
NM_001191005.2:c.274+615A>C NP_001177934.1:n.274+615A>C
NM_001191006.2:c.274+615A>C NP_001177935.1:n.274+615A>C
NM_001191007.2:c.274+615A>C NP_001177936.1:n.274+615A>C
NM_001191009.2:c.274+615A>C NP_001177938.1:n.274+615A>C
NM_001300936.1:c.274+615A>C NP_001287865.1:n.274+615A>C
NM_001300937.1:c.274+615A>C NP_001287866.1:n.274+615A>C
NM_006625.5:c.274+615A>C NP_006616.1:n.274+615A>C
NM_054016.3:c.274+615A>C NP_473357.1:n.274+615A>C
NR_034035.2:n.879+615A>C
XM_017000100.2:c.-12+615A>C XP_016855589.1:n.-12+615A>C
XM_017000101.2:c.-12+615A>C XP_016855590.1:n.-12+615A>C
XM_017000102.2:c.-12+615A>C XP_016855591.1:n.-12+615A>C
NM_001191005.3:c.274+615A>C NP_001177934.1:n.274+615A>C
NM_001191006.3:c.274+615A>C NP_001177935.1:n.274+615A>C
NM_001191007.3:c.274+615A>C NP_001177936.1:n.274+615A>C
NM_001191009.3:c.274+615A>C NP_001177938.1:n.274+615A>C
NM_001300936.2:c.274+615A>C NP_001287865.1:n.274+615A>C
NM_001300937.2:c.274+615A>C NP_001287866.1:n.274+615A>C
NM_006625.6:c.274+615A>C NP_006616.1:n.274+615A>C
NM_054016.4:c.274+615A>C MANE Select NP_473357.1:n.274+615A>C
NR_034035.3:n.743+615A>C