Canonical Allele Identifier: CA355981688

Gene: FGFR3

Linked Data

• dbSNP Id: rs2108804314
• MyVariant Identifiers: chr4:g.1807500T>A (hg19) ; chr4:g.1805773T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805773T>A , CM000666.2:g.1805773T>A	GRCh38
NC_000004.11:g.1807500T>A , CM000666.1:g.1807500T>A	GRCh37
NC_000004.10:g.1777298T>A	NCBI36
NG_012632.1:g.17462T>A , LRG_1021:g.17462T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1675T>A	ENSP00000339824.4:p.Tyr559Asn
ENST00000260795.8:c.*725T>A	ENSP00000260795.3:n.*725T>A
ENST00000352904.6:c.1333T>A	ENSP00000231803.1:p.Tyr445Asn
ENST00000412135.7:c.1657T>A	ENSP00000412903.3:p.Tyr553Asn
ENST00000440486.8:c.1669T>A MANE Select	ENSP00000414914.2:p.Tyr557Asn
ENST00000481110.7:c.1672T>A	ENSP00000420533.2:p.Tyr558Asn
ENST00000260795.6:c.1669T>A	ENSP00000260795.2:p.Tyr557Asn
ENST00000340107.8:c.1675T>A	ENSP00000339824.4:p.Tyr559Asn
ENST00000352904.5:c.1333T>A	ENSP00000231803.1:p.Tyr445Asn
ENST00000412135.6:c.1333T>A	ENSP00000412903.2:p.Tyr445Asn
ENST00000440486.6:c.1669T>A	ENSP00000414914.2:p.Tyr557Asn
ENST00000469068.1:n.735T>A
ENST00000481110.6:c.1672T>A	ENSP00000420533.2:p.Tyr558Asn
ENST00000613647.4:c.*725T>A	ENSP00000479472.1:n.*725T>A
NM_000142.4:c.1669T>A , LRG_1021t1:c.1669T>A	NP_000133.1:p.Tyr557Asn
NM_001163213.1:c.1675T>A , LRG_1021t2:c.1675T>A	NP_001156685.1:p.Tyr559Asn
NM_022965.3:c.1333T>A	NP_075254.1:p.Tyr445Asn
XM_006713868.1:c.1681T>A	XP_006713931.1:p.Tyr561Asn
XM_006713869.1:c.1681T>A	XP_006713932.1:p.Tyr561Asn
XM_006713870.1:c.1678T>A	XP_006713933.1:p.Tyr560Asn
XM_006713871.1:c.1675T>A	XP_006713934.1:p.Tyr559Asn
XM_006713872.1:c.1672T>A	XP_006713935.1:p.Tyr558Asn
XM_006713873.1:c.1669T>A	XP_006713936.1:p.Tyr557Asn
XM_011513420.1:c.1675T>A	XP_011511722.1:p.Tyr559Asn
XM_011513422.1:c.1672T>A	XP_011511724.1:p.Tyr558Asn
NM_001354809.1:c.1672T>A	NP_001341738.1:p.Tyr558Asn
NM_001354810.1:c.1672T>A	NP_001341739.1:p.Tyr558Asn
NR_148971.1:n.2076T>A
NM_001354809.2:c.1672T>A	NP_001341738.1:p.Tyr558Asn
NM_001354810.2:c.1672T>A	NP_001341739.1:p.Tyr558Asn
NR_148971.2:n.2095T>A
NM_000142.5:c.1669T>A MANE Select	NP_000133.1:p.Tyr557Asn
NM_001163213.2:c.1675T>A	NP_001156685.1:p.Tyr559Asn
NM_022965.4:c.1333T>A	NP_075254.1:p.Tyr445Asn