Canonical Allele Identifier: CA731119029

Gene: FLVCR1

Linked Data

• dbSNP Id: rs1272420868
• MyVariant Identifiers: chr1:g.213056957del (hg19) ; chr1:g.212883615del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.212883615del , CM000663.2:g.212883615del	GRCh38
NC_000001.10:g.213056957del , CM000663.1:g.213056957del	GRCh37
NC_000001.9:g.211123580del	NCBI36
NG_028131.1:g.30361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366971.9:c.1092+177del MANE Select	ENSP00000355938.4:n.1092+177del
ENST00000366971.8:c.1092+177del	ENSP00000355938.4:n.1092+177del
ENST00000419102.1:c.488+177del
ENST00000474693.1:n.317+177del
ENST00000483790.1:n.30+177del
NM_014053.3:c.1092+177del	NP_054772.1:n.1092+177del
XM_011509446.1:c.1092+177del	XP_011507748.1:n.1092+177del
XR_247024.1:n.1266+177del
XR_426771.1:n.1393+177del
XM_011509446.3:c.1092+177del	XP_011507748.1:n.1092+177del
XR_247024.3:n.1266+177del
NM_014053.4:c.1092+177del MANE Select	NP_054772.1:n.1092+177del