Canonical Allele Identifier: CA344797319
Community Standard Title: NM_014053.4(FLVCR1):c.641A>G (p.Gln214Arg)
Gene: FLVCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212859093A>G , CM000663.2:g.212859093A>G GRCh38
NC_000001.10:g.213032435A>G , CM000663.1:g.213032435A>G GRCh37
NC_000001.9:g.211099058A>G NCBI36
NG_028131.1:g.5839A>G

Transcript Alleles

HGVS Amino-acid Change
NM_014053.4:c.641A>G MANE Select NP_054772.1:p.Gln214Arg
ENST00000366971.9:c.641A>G MANE Select ENSP00000355938.4:p.Gln214Arg
NM_014053.3:c.641A>G NP_054772.1:p.Gln214Arg
ENST00000366971.8:c.641A>G ENSP00000355938.4:p.Gln214Arg
ENST00000419102.1:c.178A>G
XM_011509446.1:c.641A>G XP_011507748.1:p.Gln214Arg
XM_011509446.3:c.641A>G XP_011507748.1:p.Gln214Arg
XM_011509447.1:c.641A>G XP_011507749.1:p.Gln214Arg
XM_011509447.2:c.641A>G XP_011507749.1:p.Gln214Arg
XM_011509448.1:c.641A>G XP_011507750.1:p.Gln214Arg
XR_247024.1:n.815A>G
XR_247024.3:n.815A>G
XR_426771.1:n.815A>G
XR_426772.2:n.815A>G
XR_426772.3:n.815A>G
XR_921769.1:n.815A>G