Canonical Allele Identifier: CA423422808
Gene: FLVCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.213032157C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212858815C>T , CM000663.2:g.212858815C>T GRCh38
NC_000001.10:g.213032157C>T , CM000663.1:g.213032157C>T GRCh37
NC_000001.9:g.211098780C>T NCBI36
NG_028131.1:g.5561C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.363C>T MANE Select ENSP00000355938.4:p.Asn121=
ENST00000366971.8:c.363C>T ENSP00000355938.4:p.Asn121=
NM_014053.3:c.363C>T NP_054772.1:p.Asn121=
XM_011509446.1:c.363C>T XP_011507748.1:p.Asn121=
XM_011509447.1:c.363C>T XP_011507749.1:p.Asn121=
XM_011509448.1:c.363C>T XP_011507750.1:p.Asn121=
XR_247024.1:n.537C>T
XR_426771.1:n.537C>T
XR_426772.2:n.537C>T
XR_921769.1:n.537C>T
XM_011509446.3:c.363C>T XP_011507748.1:p.Asn121=
XM_011509447.2:c.363C>T XP_011507749.1:p.Asn121=
XR_247024.3:n.537C>T
XR_426772.3:n.537C>T
NM_014053.4:c.363C>T MANE Select NP_054772.1:p.Asn121=