Canonical Allele Identifier: CA340027
Community Standard Title: NM_013246.3(CLCF1):c.321C>A (p.Tyr107Ter)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67365493G>T , CM000673.2:g.67365493G>T GRCh38
NC_000011.9:g.67132964G>T , CM000673.1:g.67132964G>T GRCh37
NC_000011.8:g.66889540G>T NCBI36
NG_013377.1:g.13685C>A

Transcript Alleles

HGVS Amino-acid Change
NM_013246.3:c.321C>A (CLCF1) MANE Select NP_037378.1:p.Tyr107Ter
ENST00000312438.8:c.321C>A (CLCF1) MANE Select ENSP00000309338.7:p.Tyr107Ter
NM_001166212.1:c.291C>A (CLCF1) NP_001159684.1:p.Tyr97Ter
NM_001166212.2:c.291C>A (CLCF1) NP_001159684.1:p.Tyr97Ter
NM_013246.2:c.321C>A (CLCF1) NP_037378.1:p.Tyr107Ter
NR_024469.1:n.424-22042G>T
ENST00000312438.7:c.321C>A (CLCF1) ENSP00000309338.7:p.Tyr107Ter
ENST00000533438.1:c.291C>A (CLCF1) ENSP00000434122.1:p.Tyr97Ter
ENST00000543494.1:c.16+8031C>A ENSP00000480527.1:n.16+8031C>A
ENST00000622583.4:n.392-22042G>T (RAD9A)