Canonical Allele Identifier: CA918912913

Gene: FCHSD2

Linked Data

• dbSNP Id: rs3223742

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72959854_72959886delinsTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG , CM000673.2:g.72959854_72959886delinsTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	GRCh38
NC_000011.9:g.72670899_72670931delinsTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG , CM000673.1:g.72670899_72670931delinsTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	GRCh37
NC_000011.8:g.72348547_72348579delinsTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000409418.9:c.705+24202_705+24234delinsCACACACACACACACACACACACACACACACACACACACA MANE Select	ENSP00000386722.4:n.705+24202_705+24234delinsCACACACACACACACA...
ENST00000311172.11:c.537+24202_537+24234delinsCACACACACACACACACACACACACACACACACACACACA	ENSP00000308978.7:n.537+24202_537+24234delinsCACACACACACACACA...
ENST00000409314.5:c.705+24202_705+24234delinsCACACACACACACACACACACACACACACACACACACACA	ENSP00000386987.1:n.705+24202_705+24234delinsCACACACACACACACA...
ENST00000409418.8:c.705+24202_705+24234delinsCACACACACACACACACACACACACACACACACACACACA	ENSP00000386722.4:n.705+24202_705+24234delinsCACACACACACACACA...
ENST00000409853.5:c.537+24202_537+24234delinsCACACACACACACACACACACACACACACACACACACACA	ENSP00000386314.1:n.537+24202_537+24234delinsCACACACACACACACA...
ENST00000458644.6:c.225+24202_225+24234delinsCACACACACACACACACACACACACACACACACACACACA	ENSP00000402972.2:n.225+24202_225+24234delinsCACACACACACACACA...
NM_014824.2:c.705+24202_705+24234delinsCACACACACACACACACACACACACACACACACACACACA	NP_055639.2:n.705+24202_705+24234delinsCACACACACACACACACACACA...
XM_011545409.1:c.642+24202_642+24234delinsCACACACACACACACACACACACACACACACACACACACA	XP_011543711.1:n.642+24202_642+24234delinsCACACACACACACACACAC...
XM_011545410.1:c.630+24202_630+24234delinsCACACACACACACACACACACACACACACACACACACACA	XP_011543712.1:n.630+24202_630+24234delinsCACACACACACACACACAC...
XM_011545411.1:c.471+24202_471+24234delinsCACACACACACACACACACACACACACACACACACACACA	XP_011543713.1:n.471+24202_471+24234delinsCACACACACACACACACAC...
XM_011545412.1:c.705+24202_705+24234delinsCACACACACACACACACACACACACACACACACACACACA	XP_011543714.1:n.705+24202_705+24234delinsCACACACACACACACACAC...
XM_011545410.2:c.630+24202_630+24234delinsCACACACACACACACACACACACACACACACACACACACA	XP_011543712.1:n.630+24202_630+24234delinsCACACACACACACACACAC...
XM_017018632.1:c.642+24202_642+24234delinsCACACACACACACACACACACACACACACACACACACACA	XP_016874121.1:n.642+24202_642+24234delinsCACACACACACACACACAC...
XR_001748055.1:n.1510+24202_1510+24234delinsCACACACACACACACACACACACACACACACACACACACA
NM_014824.3:c.705+24202_705+24234delinsCACACACACACACACACACACACACACACACACACACACA MANE Select	NP_055639.2:n.705+24202_705+24234delinsCACACACACACACACACACACA...