Canonical Allele Identifier: CA14964041
Community Standard Title: NM_182895.5(SCARF2):c.174-213T>G
Gene: SCARF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20432201A>C , CM000684.2:g.20432201A>C GRCh38
NC_000022.10:g.20786488A>C , CM000684.1:g.20786488A>C GRCh37
NC_000022.9:g.19116488A>C NCBI36
NG_031868.2:g.10659T>G

Transcript Alleles

HGVS Amino-acid Change
NM_182895.5:c.174-213T>G MANE Select NP_878315.2:n.174-213T>G
ENST00000622235.5:c.174-213T>G MANE Select ENSP00000477564.2:n.174-213T>G
NM_153334.6:c.174-213T>G NP_699165.3:n.174-213T>G
NM_153334.7:c.174-213T>G NP_699165.3:n.174-213T>G
NM_182895.4:c.174-213T>G NP_878315.2:n.174-213T>G
ENST00000429594.1:c.179-1644T>G
ENST00000615031.4:c.174-213T>G ENSP00000479389.1:n.174-213T>G
ENST00000622235.4:c.174-213T>G ENSP00000477564.1:n.174-213T>G
ENST00000623402.1:c.174-213T>G ENSP00000485276.1:n.174-213T>G
XM_017029065.2:c.174-213T>G XP_016884554.1:n.174-213T>G