Canonical Allele Identifier: CA2810566
Community Standard Title: NM_000142.5(FGFR3):c.1753C>T (p.Pro585Ser)
Gene: FGFR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1805857C>T , CM000666.2:g.1805857C>T GRCh38
NC_000004.11:g.1807584C>T , CM000666.1:g.1807584C>T GRCh37
NC_000004.10:g.1777382C>T NCBI36
NG_012632.1:g.17546C>T , LRG_1021:g.17546C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000142.5:c.1753C>T MANE Select NP_000133.1:p.Pro585Ser
ENST00000440486.8:c.1753C>T MANE Select ENSP00000414914.2:p.Pro585Ser
NM_000142.4:c.1753C>T , LRG_1021t1:c.1753C>T NP_000133.1:p.Pro585Ser
NM_001163213.1:c.1759C>T , LRG_1021t2:c.1759C>T NP_001156685.1:p.Pro587Ser
NM_001163213.2:c.1759C>T NP_001156685.1:p.Pro587Ser
NM_001354809.1:c.1756C>T NP_001341738.1:p.Pro586Ser
NM_001354809.2:c.1756C>T NP_001341738.1:p.Pro586Ser
NM_001354810.1:c.1756C>T NP_001341739.1:p.Pro586Ser
NM_001354810.2:c.1756C>T NP_001341739.1:p.Pro586Ser
NM_022965.3:c.1417C>T NP_075254.1:p.Pro473Ser
NM_022965.4:c.1417C>T NP_075254.1:p.Pro473Ser
NR_148971.1:n.2160C>T
NR_148971.2:n.2179C>T
ENST00000260795.6:c.1753C>T ENSP00000260795.2:p.Pro585Ser
ENST00000260795.8:c.*809C>T ENSP00000260795.3:n.*809C>T
ENST00000340107.8:c.1759C>T ENSP00000339824.4:p.Pro587Ser
ENST00000340107.9:c.1759C>T ENSP00000339824.4:p.Pro587Ser
ENST00000352904.5:c.1417C>T ENSP00000231803.1:p.Pro473Ser
ENST00000352904.6:c.1417C>T ENSP00000231803.1:p.Pro473Ser
ENST00000412135.6:c.1417C>T ENSP00000412903.2:p.Pro473Ser
ENST00000412135.7:c.1741C>T ENSP00000412903.3:p.Pro581Ser
ENST00000440486.6:c.1753C>T ENSP00000414914.2:p.Pro585Ser
ENST00000469068.1:n.819C>T
ENST00000481110.6:c.1756C>T ENSP00000420533.2:p.Pro586Ser
ENST00000481110.7:c.1756C>T ENSP00000420533.2:p.Pro586Ser
ENST00000613647.4:c.*809C>T ENSP00000479472.1:n.*809C>T
XM_006713868.1:c.1765C>T XP_006713931.1:p.Pro589Ser
XM_006713869.1:c.1765C>T XP_006713932.1:p.Pro589Ser
XM_006713870.1:c.1762C>T XP_006713933.1:p.Pro588Ser
XM_006713871.1:c.1759C>T XP_006713934.1:p.Pro587Ser
XM_006713872.1:c.1756C>T XP_006713935.1:p.Pro586Ser
XM_006713873.1:c.1753C>T XP_006713936.1:p.Pro585Ser
XM_011513420.1:c.1759C>T XP_011511722.1:p.Pro587Ser
XM_011513422.1:c.1756C>T XP_011511724.1:p.Pro586Ser