Canonical Allele Identifier: CA1604713515

Gene: FLT4

Linked Data

• dbSNP Id: rs1761565215
• gnomAD v3: 5-180602486-AAC-A
• gnomAD v4: 5-180602486-AAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180602488_180602489del , CM000667.2:g.180602488_180602489del	GRCh38
NC_000005.9:g.180029488_180029489del , CM000667.1:g.180029488_180029489del	GRCh37
NC_000005.8:g.179962094_179962095del	NCBI36
NG_011536.1:g.52137_52138del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.*704_*705del MANE Select	ENSP00000261937.6:n.*704_*705del
ENST00000261937.10:c.*704_*705del	ENSP00000261937.6:n.*704_*705del
NM_182925.4:c.*704_*705del	NP_891555.2:n.*704_*705del
XM_011534477.1:c.*704_*705del	XP_011532779.1:n.*704_*705del
XM_011534478.1:c.*704_*705del	XP_011532780.1:n.*704_*705del
XM_011534482.1:c.*704_*705del	XP_011532784.1:n.*704_*705del
XM_011534483.1:c.*704_*705del	XP_011532785.1:n.*704_*705del
XM_011534484.1:c.*704_*705del	XP_011532786.1:n.*704_*705del
XM_011534478.3:c.*704_*705del	XP_011532780.1:n.*704_*705del
XM_011534484.2:c.*704_*705del	XP_011532786.1:n.*704_*705del
XM_017009263.1:c.*942_*943del	XP_016864752.1:n.*942_*943del
XM_017009268.1:c.*704_*705del	XP_016864757.1:n.*704_*705del
XR_001742050.2:n.5286_5287del
NM_182925.5:c.*704_*705del MANE Select	NP_891555.2:n.*704_*705del