Canonical Allele Identifier: CA2485643526

Gene: FLVCR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.212883735_212883736delinsCA , CM000663.2:g.212883735_212883736delinsCA	GRCh38
NC_000001.10:g.213057077_213057078delinsCA , CM000663.1:g.213057077_213057078delinsCA	GRCh37
NC_000001.9:g.211123700_211123701delinsCA	NCBI36
NG_028131.1:g.30481_30482delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366971.9:c.1092+297_1092+298delinsCA MANE Select	ENSP00000355938.4:n.1092+297_1092+298delinsCA
ENST00000366971.8:c.1092+297_1092+298delinsCA	ENSP00000355938.4:n.1092+297_1092+298delinsCA
ENST00000419102.1:c.488+297_488+298delinsCA
ENST00000474693.1:n.317+297_317+298delinsCA
ENST00000483790.1:n.30+297_30+298delinsCA
NM_014053.3:c.1092+297_1092+298delinsCA	NP_054772.1:n.1092+297_1092+298delinsCA
XM_011509446.1:c.1092+297_1092+298delinsCA	XP_011507748.1:n.1092+297_1092+298delinsCA
XR_247024.1:n.1266+297_1266+298delinsCA
XR_426771.1:n.1393+297_1393+298delinsCA
XM_011509446.3:c.1092+297_1092+298delinsCA	XP_011507748.1:n.1092+297_1092+298delinsCA
XR_247024.3:n.1266+297_1266+298delinsCA
NM_014053.4:c.1092+297_1092+298delinsCA MANE Select	NP_054772.1:n.1092+297_1092+298delinsCA