Canonical Allele Identifier: CA3605600

Gene: FLT4

Linked Data

• ClinVar Variation Id: 2307716
• ClinVar RCV Id: RCV002900788
• dbSNP Id: rs759044121
• ExAC: 5:180030283 T / C
• gnomAD v2: 5-180030283-T-C
• gnomAD v3: 5-180603283-T-C
• gnomAD v4: 5-180603283-T-C
• MyVariant Identifiers: chr5:g.180030283T>C (hg19) ; chr5:g.180603283T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603283T>C , CM000667.2:g.180603283T>C	GRCh38
NC_000005.9:g.180030283T>C , CM000667.1:g.180030283T>C	GRCh37
NC_000005.8:g.179962889T>C	NCBI36
NG_011536.1:g.51342A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4001A>G MANE Select	ENSP00000261937.6:p.Asn1334Ser
ENST00000261937.10:c.4001A>G	ENSP00000261937.6:p.Asn1334Ser
ENST00000502603.5:n.701A>G
NM_182925.4:c.4001A>G	NP_891555.2:p.Asn1334Ser
XM_011534477.1:c.4250A>G	XP_011532779.1:p.Asn1417Ser
XM_011534478.1:c.4232A>G	XP_011532780.1:p.Asn1411Ser
XM_011534482.1:c.4019A>G	XP_011532784.1:p.Asn1340Ser
XM_011534483.1:c.3941A>G	XP_011532785.1:p.Asn1314Ser
XM_011534484.1:c.3542A>G	XP_011532786.1:p.Asn1181Ser
XR_941095.1:n.4287A>G
XM_011534478.3:c.4232A>G	XP_011532780.1:p.Asn1411Ser
XM_011534484.2:c.3542A>G	XP_011532786.1:p.Asn1181Ser
XM_017009263.1:c.*147A>G	XP_016864752.1:n.*147A>G
XM_017009268.1:c.3923A>G	XP_016864757.1:p.Asn1308Ser
XR_001742050.2:n.4491A>G
NM_182925.5:c.4001A>G MANE Select	NP_891555.2:p.Asn1334Ser