Canonical Allele Identifier: CA1980082846
Community Standard Title: NM_013246.3(CLCF1):c.321C= (p.Tyr107=)

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_013246.3:c.321C= (CLCF1) MANE Select NP_037378.1:p.Tyr107=
ENST00000312438.8:c.321C= (CLCF1) MANE Select ENSP00000309338.7:p.Tyr107=
NM_001166212.1:c.291C= (CLCF1) NP_001159684.1:p.Tyr97=
NM_001166212.2:c.291C= (CLCF1) NP_001159684.1:p.Tyr97=
NM_013246.2:c.321C= (CLCF1) NP_037378.1:p.Tyr107=
NR_024469.1:n.424-22042G=
ENST00000312438.7:c.321C= (CLCF1) ENSP00000309338.7:p.Tyr107=
ENST00000533438.1:c.291C= (CLCF1) ENSP00000434122.1:p.Tyr97=
ENST00000543494.1:c.16+8031C= ENSP00000480527.1:n.16+8031C=
ENST00000622583.4:n.392-22042G= (RAD9A)