Canonical Allele Identifier: CA2711055316

Gene: FLT4

Linked Data

• dbSNP Id: rs2127781560

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603186T>G , CM000667.2:g.180603186T>G	GRCh38
NC_000005.9:g.180030186T>G , CM000667.1:g.180030186T>G	GRCh37
NC_000005.8:g.179962792T>G	NCBI36
NG_011536.1:g.51439A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.*6A>C MANE Select	ENSP00000261937.6:n.*6A>C
ENST00000261937.10:c.*6A>C	ENSP00000261937.6:n.*6A>C
ENST00000502603.5:n.798A>C
NM_182925.4:c.*6A>C	NP_891555.2:n.*6A>C
XM_011534477.1:c.*6A>C	XP_011532779.1:n.*6A>C
XM_011534478.1:c.*6A>C	XP_011532780.1:n.*6A>C
XM_011534482.1:c.*6A>C	XP_011532784.1:n.*6A>C
XM_011534483.1:c.*6A>C	XP_011532785.1:n.*6A>C
XM_011534484.1:c.*6A>C	XP_011532786.1:n.*6A>C
XR_941095.1:n.4384A>C
XM_011534478.3:c.*6A>C	XP_011532780.1:n.*6A>C
XM_011534484.2:c.*6A>C	XP_011532786.1:n.*6A>C
XM_017009263.1:c.*244A>C	XP_016864752.1:n.*244A>C
XM_017009268.1:c.*6A>C	XP_016864757.1:n.*6A>C
XR_001742050.2:n.4588A>C
NM_182925.5:c.*6A>C MANE Select	NP_891555.2:n.*6A>C