Canonical Allele Identifier: CA1480044628

Gene: C4orf17

Linked Data

• dbSNP Id: rs13126513

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99523527T>G , CM000666.2:g.99523527T>G	GRCh38
NC_000004.11:g.100444684T>G , CM000666.1:g.100444684T>G	GRCh37
NC_000004.10:g.100663707T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000326581.9:c.337+818T>G MANE Select	ENSP00000322582.4:n.337+818T>G
ENST00000326581.8:c.337+818T>G	ENSP00000322582.4:n.337+818T>G
ENST00000477187.1:c.337+818T>G	ENSP00000423411.1:n.337+818T>G
ENST00000503257.1:n.334+818T>G
ENST00000514652.5:c.337+818T>G	ENSP00000427663.1:n.337+818T>G
NM_032149.2:c.337+818T>G	NP_115525.2:n.337+818T>G
XM_011532315.1:c.337+818T>G	XP_011530617.1:n.337+818T>G
XM_011532315.2:c.337+818T>G	XP_011530617.1:n.337+818T>G
NM_032149.3:c.337+818T>G MANE Select	NP_115525.2:n.337+818T>G