Canonical Allele Identifier: CA1740760
Gene: CAPG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85398769T>C , CM000664.2:g.85398769T>C GRCh38
NC_000002.11:g.85625892T>C , CM000664.1:g.85625892T>C GRCh37
NC_000002.10:g.85479403T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001747.4:c.680A>G MANE Select NP_001738.2:p.Lys227Arg
ENST00000263867.9:c.680A>G MANE Select ENSP00000263867.4:p.Lys227Arg
NM_001256139.1:c.680A>G NP_001243068.1:p.Lys227Arg
NM_001256139.2:c.680A>G NP_001243068.1:p.Lys227Arg
NM_001256140.1:c.635A>G NP_001243069.1:p.Lys212Arg
NM_001256140.2:c.635A>G NP_001243069.1:p.Lys212Arg
NM_001320732.1:c.680A>G NP_001307661.1:p.Lys227Arg
NM_001320732.2:c.680A>G NP_001307661.1:p.Lys227Arg
NM_001320733.1:c.680A>G NP_001307662.1:p.Lys227Arg
NM_001320733.2:c.680A>G NP_001307662.1:p.Lys227Arg
NM_001320734.1:c.666+367A>G NP_001307663.1:n.666+367A>G
NM_001320734.2:c.666+367A>G NP_001307663.1:n.666+367A>G
NM_001747.3:c.680A>G NP_001738.2:p.Lys227Arg
ENST00000263867.8:c.680A>G ENSP00000263867.4:p.Lys227Arg
ENST00000409670.5:c.680A>G ENSP00000386315.1:p.Lys227Arg
ENST00000409724.5:c.680A>G ENSP00000386965.1:p.Lys227Arg
ENST00000409921.5:c.635A>G ENSP00000387063.1:p.Lys212Arg
ENST00000439385.5:c.680A>G ENSP00000391923.1:p.Lys227Arg
ENST00000447219.6:c.680A>G ENSP00000398232.2:p.Lys227Arg
ENST00000449030.5:c.680A>G ENSP00000403330.1:p.Lys227Arg
ENST00000459793.2:n.894A>G
ENST00000483659.5:n.472A>G
XM_005264581.2:c.680A>G XP_005264638.1:p.Lys227Arg
XM_011533122.1:c.680A>G XP_011531424.1:p.Lys227Arg
XM_011533123.1:c.680A>G XP_011531425.1:p.Lys227Arg