Canonical Allele Identifier: CA808406622

Gene: FLT4

Linked Data

• dbSNP Id: rs1441543226
• gnomAD v3: 5-180641673-T-C
• gnomAD v4: 5-180641673-T-C
• MyVariant Identifiers: chr5:g.180068673T>C (hg19) ; chr5:g.180641673T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180641673T>C , CM000667.2:g.180641673T>C	GRCh38
NC_000005.9:g.180068673T>C , CM000667.1:g.180068673T>C	GRCh37
NC_000005.8:g.180001279T>C	NCBI36
NG_011536.1:g.12952A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261937.11:c.58+7815A>G MANE Select	ENSP00000261937.6:n.58+7815A>G
ENST00000261937.10:c.58+7815A>G	ENSP00000261937.6:n.58+7815A>G
ENST00000393347.7:c.58+7815A>G	ENSP00000377016.3:n.58+7815A>G
ENST00000424276.6:n.58+7815A>G
ENST00000502293.5:n.58+7815A>G
ENST00000502649.5:c.58+7815A>G	ENSP00000426057.1:n.58+7815A>G
ENST00000513527.1:n.58+7815A>G
ENST00000619105.4:c.58+7815A>G	ENSP00000481134.1:n.58+7815A>G
NM_002020.4:c.58+7815A>G	NP_002011.2:n.58+7815A>G
NM_182925.4:c.58+7815A>G	NP_891555.2:n.58+7815A>G
XM_011534477.1:c.289+3194A>G	XP_011532779.1:n.289+3194A>G
XM_011534478.1:c.289+3194A>G	XP_011532780.1:n.289+3194A>G
XM_011534479.1:c.289+3194A>G	XP_011532781.1:n.289+3194A>G
XM_011534480.1:c.289+3194A>G	XP_011532782.1:n.289+3194A>G
XM_011534481.1:c.289+3194A>G	XP_011532783.1:n.289+3194A>G
XM_011534482.1:c.58+7815A>G	XP_011532784.1:n.58+7815A>G
XM_011534483.1:c.-21+8546A>G	XP_011532785.1:n.-21+8546A>G
XR_941095.1:n.301+3194A>G
NM_001354989.1:c.58+7815A>G	NP_001341918.1:n.58+7815A>G
XM_011534478.3:c.289+3194A>G	XP_011532780.1:n.289+3194A>G
XM_017009263.1:c.289+3194A>G	XP_016864752.1:n.289+3194A>G
XM_017009264.2:c.289+3194A>G	XP_016864753.1:n.289+3194A>G
XM_017009265.1:c.289+3194A>G	XP_016864754.1:n.289+3194A>G
XM_017009266.1:c.289+3194A>G	XP_016864755.1:n.289+3194A>G
XM_017009267.2:c.289+3194A>G	XP_016864756.1:n.289+3194A>G
XM_017009268.1:c.-21+8546A>G	XP_016864757.1:n.-21+8546A>G
XR_001742050.2:n.523+3194A>G
NM_182925.5:c.58+7815A>G MANE Select	NP_891555.2:n.58+7815A>G
NM_001354989.2:c.58+7815A>G	NP_001341918.1:n.58+7815A>G
NM_002020.5:c.58+7815A>G	NP_002011.2:n.58+7815A>G