Canonical Allele Identifier: CA2056438916
Gene: CCDC38 HGNC NCBI
SNRPF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95895091G= , CM000674.2:g.95895091G= GRCh38
NC_000012.11:g.96288869G= , CM000674.1:g.96288869G= GRCh37
NC_000012.10:g.94813000G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344280.8:c.670C= (CCDC38) MANE Select ENSP00000345470.3:p.Leu224=
ENST00000344280.7:c.670C= (CCDC38) ENSP00000345470.3:p.Leu224=
ENST00000552085.1:c.286+5910G= (SNRPF) ENSP00000447127.1:n.286+5910G=
NM_182496.2:c.670C= (CCDC38) NP_872302.2:p.Leu224=
XM_006719229.1:c.178C= (CCDC38) XP_006719292.1:p.Leu60=
XM_011537883.1:c.670C= (CCDC38) XP_011536185.1:p.Leu224=
XM_011537884.1:c.550C= (CCDC38) XP_011536186.1:p.Leu184=
XM_011537885.1:c.550C= (CCDC38) XP_011536187.1:p.Leu184=
XM_011537886.1:c.550C= (CCDC38) XP_011536188.1:p.Leu184=
XM_011537887.1:c.550C= (CCDC38) XP_011536189.1:p.Leu184=
XM_011537888.1:c.19C= (CCDC38) XP_011536190.1:p.Leu7=
XM_011537889.1:c.670C= (CCDC38) XP_011536191.1:p.Leu224=
XR_429080.1:n.902C= (CCDC38)
XM_006719229.2:c.178C= (CCDC38) XP_006719292.1:p.Leu60=
XM_011537883.2:c.670C= (CCDC38) XP_011536185.1:p.Leu224=
XM_011537884.2:c.550C= (CCDC38) XP_011536186.1:p.Leu184=
XM_011537886.2:c.550C= (CCDC38) XP_011536188.1:p.Leu184=
XM_011537887.2:c.550C= (CCDC38) XP_011536189.1:p.Leu184=
XM_011537888.3:c.19C= (CCDC38) XP_011536190.1:p.Leu7=
NM_182496.3:c.670C= (CCDC38) MANE Select NP_872302.2:p.Leu224=