Canonical Allele Identifier: CA1433507495

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805582T= , CM000666.2:g.1805582T=	GRCh38
NC_000004.11:g.1807309T= , CM000666.1:g.1807309T=	GRCh37
NC_000004.10:g.1777107T=	NCBI36
NG_012632.1:g.17271T= , LRG_1021:g.17271T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1564T=	ENSP00000339824.4:p.Ser522=
ENST00000260795.8:c.*614T=	ENSP00000260795.3:n.*614T=
ENST00000352904.6:c.1222T=	ENSP00000231803.1:p.Ser408=
ENST00000412135.7:c.1546T=	ENSP00000412903.3:p.Ser516=
ENST00000440486.8:c.1558T= MANE Select	ENSP00000414914.2:p.Ser520=
ENST00000481110.7:c.1561T=	ENSP00000420533.2:p.Ser521=
ENST00000260795.6:c.1558T=	ENSP00000260795.2:p.Ser520=
ENST00000340107.8:c.1564T=	ENSP00000339824.4:p.Ser522=
ENST00000352904.5:c.1222T=	ENSP00000231803.1:p.Ser408=
ENST00000412135.6:c.1222T=	ENSP00000412903.2:p.Ser408=
ENST00000440486.6:c.1558T=	ENSP00000414914.2:p.Ser520=
ENST00000469068.1:n.624T=
ENST00000481110.6:c.1561T=	ENSP00000420533.2:p.Ser521=
ENST00000613647.4:c.*614T=	ENSP00000479472.1:n.*614T=
NM_000142.4:c.1558T= , LRG_1021t1:c.1558T=	NP_000133.1:p.Ser520=
NM_001163213.1:c.1564T= , LRG_1021t2:c.1564T=	NP_001156685.1:p.Ser522=
NM_022965.3:c.1222T=	NP_075254.1:p.Ser408=
XM_006713868.1:c.1570T=	XP_006713931.1:p.Ser524=
XM_006713869.1:c.1570T=	XP_006713932.1:p.Ser524=
XM_006713870.1:c.1567T=	XP_006713933.1:p.Ser523=
XM_006713871.1:c.1564T=	XP_006713934.1:p.Ser522=
XM_006713872.1:c.1561T=	XP_006713935.1:p.Ser521=
XM_006713873.1:c.1558T=	XP_006713936.1:p.Ser520=
XM_011513420.1:c.1564T=	XP_011511722.1:p.Ser522=
XM_011513422.1:c.1561T=	XP_011511724.1:p.Ser521=
NM_001354809.1:c.1561T=	NP_001341738.1:p.Ser521=
NM_001354810.1:c.1561T=	NP_001341739.1:p.Ser521=
NR_148971.1:n.1965T=
NM_001354809.2:c.1561T=	NP_001341738.1:p.Ser521=
NM_001354810.2:c.1561T=	NP_001341739.1:p.Ser521=
NR_148971.2:n.1984T=
NM_000142.5:c.1558T= MANE Select	NP_000133.1:p.Ser520=
NM_001163213.2:c.1564T=	NP_001156685.1:p.Ser522=
NM_022965.4:c.1222T=	NP_075254.1:p.Ser408=