Canonical Allele Identifier: CA1980086581
Community Standard Title: NM_013246.3(CLCF1):c.46T= (p.Cys16=)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67367597A= , CM000673.2:g.67367597A= GRCh38
NC_000011.9:g.67135068A= , CM000673.1:g.67135068A= GRCh37
NC_000011.8:g.66891644A= NCBI36
NG_013377.1:g.11581T=

Transcript Alleles

HGVS Amino-acid Change
NM_013246.3:c.46T= (CLCF1) MANE Select NP_037378.1:p.Cys16=
ENST00000312438.8:c.46T= (CLCF1) MANE Select ENSP00000309338.7:p.Cys16=
NM_001166212.1:c.16T= (CLCF1) NP_001159684.1:p.Cys6=
NM_001166212.2:c.16T= (CLCF1) NP_001159684.1:p.Cys6=
NM_013246.2:c.46T= (CLCF1) NP_037378.1:p.Cys16=
NR_024469.1:n.424-19938A=
ENST00000312438.7:c.46T= (CLCF1) ENSP00000309338.7:p.Cys16=
ENST00000533438.1:c.16T= (CLCF1) ENSP00000434122.1:p.Cys6=
ENST00000543494.1:c.16+5927T= ENSP00000480527.1:n.16+5927T=
ENST00000622583.4:n.392-19938A= (RAD9A)