Canonical Allele Identifier: CA10338742

Gene: ARSF

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.3072032C>G , CM000685.2:g.3072032C>G	GRCh38
NC_000023.10:g.2990073C>G , CM000685.1:g.2990073C>G	GRCh37
NC_000023.9:g.3000073C>G	NCBI36
NG_012822.2:g.36799C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381127.6:c.18C>G MANE Select	ENSP00000370519.1:p.Pro6=
ENST00000359361.2:c.18C>G	ENSP00000352319.2:p.Pro6=
ENST00000381127.5:c.18C>G	ENSP00000370519.1:p.Pro6=
NM_001201538.1:c.18C>G	NP_001188467.1:p.Pro6=
NM_001201539.1:c.18C>G	NP_001188468.1:p.Pro6=
NM_004042.4:c.18C>G	NP_004033.2:p.Pro6=
XM_011545522.1:c.69C>G	XP_011543824.1:p.Pro23=
XM_011545523.1:c.69C>G	XP_011543825.1:p.Pro23=
XM_011545524.1:c.69C>G	XP_011543826.1:p.Pro23=
XM_017029527.1:c.18C>G	XP_016885016.1:p.Pro6=
XM_017029528.1:c.69C>G	XP_016885017.1:p.Pro23=
NM_001201539.2:c.18C>G MANE Select	NP_001188468.1:p.Pro6=
NM_001201538.2:c.18C>G	NP_001188467.1:p.Pro6=
NM_004042.5:c.18C>G	NP_004033.2:p.Pro6=