Canonical Allele Identifier: CA341420

Gene: FGFR3

Linked Data

• ClinVar Variation Id: 16349
• ClinVar RCV Id: RCV000017758 ; RCV000623459 ; RCV001269614 ; RCV002262566 ; RCV002273934
• dbSNP Id: rs77722678
• ExAC: 4:1807370 A / G
• gnomAD v2: 4-1807370-A-G
• gnomAD v3: 4-1805643-A-G
• gnomAD v4: 4-1805643-A-G
• MyVariant Identifiers: chr4:g.1807370A>G (hg19) ; chr4:g.1805643A>G (hg38)
• CIViC: CA341420
• PubMed: PMID:1956068 ; PMID:4078868 ; PMID:7670477 ; PMID:7847369 ; PMID:8845844 ; PMID:9450868 ; PMID:9580776 ; PMID:9677066 ; PMID:9950359 ; PMID:10053006 ; PMID:10213050 ; PMID:10602123 ; PMID:10777366 ; PMID:12707965 ; PMID:15241680 ; PMID:16501574 ; PMID:17033969 ; PMID:17935505 ; PMID:17950653 ; PMID:18000976 ; PMID:18328977 ; PMID:18344207 ; PMID:19098178 ; PMID:19449410 ; PMID:20301650 ; PMID:22045636 ; PMID:22604720 ; PMID:23378035 ; PMID:23740942 ; PMID:24864036 ; PMID:25356217 ; PMID:25931420 ; PMID:26028288 ; PMID:26740388

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805643A>G , CM000666.2:g.1805643A>G	GRCh38
NC_000004.11:g.1807370A>G , CM000666.1:g.1807370A>G	GRCh37
NC_000004.10:g.1777168A>G	NCBI36
NG_012632.1:g.17332A>G , LRG_1021:g.17332A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1625A>G	ENSP00000339824.4:p.Asn542Ser
ENST00000260795.8:c.*675A>G	ENSP00000260795.3:n.*675A>G
ENST00000352904.6:c.1283A>G	ENSP00000231803.1:p.Asn428Ser
ENST00000412135.7:c.1607A>G	ENSP00000412903.3:p.Asn536Ser
ENST00000440486.8:c.1619A>G MANE Select	ENSP00000414914.2:p.Asn540Ser
ENST00000481110.7:c.1622A>G	ENSP00000420533.2:p.Asn541Ser
ENST00000260795.6:c.1619A>G	ENSP00000260795.2:p.Asn540Ser
ENST00000340107.8:c.1625A>G	ENSP00000339824.4:p.Asn542Ser
ENST00000352904.5:c.1283A>G	ENSP00000231803.1:p.Asn428Ser
ENST00000412135.6:c.1283A>G	ENSP00000412903.2:p.Asn428Ser
ENST00000440486.6:c.1619A>G	ENSP00000414914.2:p.Asn540Ser
ENST00000469068.1:n.685A>G
ENST00000481110.6:c.1622A>G	ENSP00000420533.2:p.Asn541Ser
ENST00000613647.4:c.*675A>G	ENSP00000479472.1:n.*675A>G
NM_000142.4:c.1619A>G , LRG_1021t1:c.1619A>G	NP_000133.1:p.Asn540Ser
NM_001163213.1:c.1625A>G , LRG_1021t2:c.1625A>G	NP_001156685.1:p.Asn542Ser
NM_022965.3:c.1283A>G	NP_075254.1:p.Asn428Ser
XM_006713868.1:c.1631A>G	XP_006713931.1:p.Asn544Ser
XM_006713869.1:c.1631A>G	XP_006713932.1:p.Asn544Ser
XM_006713870.1:c.1628A>G	XP_006713933.1:p.Asn543Ser
XM_006713871.1:c.1625A>G	XP_006713934.1:p.Asn542Ser
XM_006713872.1:c.1622A>G	XP_006713935.1:p.Asn541Ser
XM_006713873.1:c.1619A>G	XP_006713936.1:p.Asn540Ser
XM_011513420.1:c.1625A>G	XP_011511722.1:p.Asn542Ser
XM_011513422.1:c.1622A>G	XP_011511724.1:p.Asn541Ser
NM_001354809.1:c.1622A>G	NP_001341738.1:p.Asn541Ser
NM_001354810.1:c.1622A>G	NP_001341739.1:p.Asn541Ser
NR_148971.1:n.2026A>G
NM_001354809.2:c.1622A>G	NP_001341738.1:p.Asn541Ser
NM_001354810.2:c.1622A>G	NP_001341739.1:p.Asn541Ser
NR_148971.2:n.2045A>G
NM_000142.5:c.1619A>G MANE Select	NP_000133.1:p.Asn540Ser
NM_001163213.2:c.1625A>G	NP_001156685.1:p.Asn542Ser
NM_022965.4:c.1283A>G	NP_075254.1:p.Asn428Ser