Canonical Allele Identifier: CA309982136
Community Standard Title: NM_002000.4(FCAR):c.767A>G (p.Asn256Ser)
Gene: FCAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54889766A>G , CM000681.2:g.54889766A>G GRCh38
NC_000019.8:g.60092944A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002000.4:c.767A>G MANE Select NP_001991.1:p.Asn256Ser
ENST00000355524.8:c.767A>G MANE Select ENSP00000347714.3:p.Asn256Ser
NM_002000.3:c.767A>G NP_001991.1:p.Asn256Ser
NM_133269.3:c.701A>G NP_579803.1:p.Asn234Ser
NM_133269.4:c.701A>G NP_579803.1:p.Asn234Ser
NM_133271.3:c.479A>G NP_579805.1:p.Asn160Ser
NM_133271.4:c.479A>G NP_579805.1:p.Asn160Ser
NM_133272.3:c.731A>G NP_579806.1:p.Asn244Ser
NM_133272.4:c.731A>G NP_579806.1:p.Asn244Ser
NM_133273.3:c.443A>G NP_579807.1:p.Asn148Ser
NM_133273.4:c.443A>G NP_579807.1:p.Asn148Ser
NM_133274.3:c.*27A>G NP_579808.1:n.*27A>G
NM_133274.4:c.*27A>G NP_579808.1:n.*27A>G
NM_133277.3:c.440A>G NP_579811.1:p.Asn147Ser
NM_133277.4:c.440A>G NP_579811.1:p.Asn147Ser
NM_133278.3:c.665A>G NP_579812.1:p.Asn222Ser
NM_133278.4:c.665A>G NP_579812.1:p.Asn222Ser
ENST00000345937.8:c.479A>G ENSP00000338257.4:p.Asn160Ser
ENST00000353758.8:c.440A>G ENSP00000338058.4:p.Asn147Ser
ENST00000355524.7:c.767A>G ENSP00000347714.3:p.Asn256Ser
ENST00000359272.8:c.731A>G ENSP00000352218.4:p.Asn244Ser
ENST00000391723.7:c.657A>G ENSP00000375603.3:n.657A>G
ENST00000391724.3:c.665A>G ENSP00000375604.3:p.Asn222Ser
ENST00000391725.7:c.701A>G ENSP00000375605.3:p.Asn234Ser
ENST00000391726.7:c.443A>G ENSP00000375606.3:p.Asn148Ser
ENST00000471750.2:n.557A>G
ENST00000472634.6:n.531A>G
ENST00000482092.6:n.779A>G
XM_011526625.1:c.686A>G XP_011524927.1:p.Asn229Ser
XM_011526625.3:c.686A>G XP_011524927.1:p.Asn229Ser
XM_011526626.1:c.686A>G XP_011524928.1:p.Asn229Ser
XM_017026473.1:c.686A>G XP_016881962.1:p.Asn229Ser
XM_017026474.2:c.686A>G XP_016881963.1:p.Asn229Ser