Canonical Allele Identifier: CA1982223164

Gene: FCHSD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72959856_72959857delinsGT , CM000673.2:g.72959856_72959857delinsGT	GRCh38
NC_000011.9:g.72670901_72670902delinsGT , CM000673.1:g.72670901_72670902delinsGT	GRCh37
NC_000011.8:g.72348549_72348550delinsGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409418.9:c.705+24231_705+24232delinsAC MANE Select	ENSP00000386722.4:n.705+24231_705+24232delinsAC
ENST00000311172.11:c.537+24231_537+24232delinsAC	ENSP00000308978.7:n.537+24231_537+24232delinsAC
ENST00000409314.5:c.705+24231_705+24232delinsAC	ENSP00000386987.1:n.705+24231_705+24232delinsAC
ENST00000409418.8:c.705+24231_705+24232delinsAC	ENSP00000386722.4:n.705+24231_705+24232delinsAC
ENST00000409853.5:c.537+24231_537+24232delinsAC	ENSP00000386314.1:n.537+24231_537+24232delinsAC
ENST00000458644.6:c.225+24231_225+24232delinsAC	ENSP00000402972.2:n.225+24231_225+24232delinsAC
NM_014824.2:c.705+24231_705+24232delinsAC	NP_055639.2:n.705+24231_705+24232delinsAC
XM_011545409.1:c.642+24231_642+24232delinsAC	XP_011543711.1:n.642+24231_642+24232delinsAC
XM_011545410.1:c.630+24231_630+24232delinsAC	XP_011543712.1:n.630+24231_630+24232delinsAC
XM_011545411.1:c.471+24231_471+24232delinsAC	XP_011543713.1:n.471+24231_471+24232delinsAC
XM_011545412.1:c.705+24231_705+24232delinsAC	XP_011543714.1:n.705+24231_705+24232delinsAC
XM_011545410.2:c.630+24231_630+24232delinsAC	XP_011543712.1:n.630+24231_630+24232delinsAC
XM_017018632.1:c.642+24231_642+24232delinsAC	XP_016874121.1:n.642+24231_642+24232delinsAC
XR_001748055.1:n.1510+24231_1510+24232delinsAC
NM_014824.3:c.705+24231_705+24232delinsAC MANE Select	NP_055639.2:n.705+24231_705+24232delinsAC