Canonical Allele Identifier: CA747496675

Gene: C21orf91

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17806954C>G , CM000683.2:g.17806954C>G	GRCh38
NC_000021.8:g.19179271C>G , CM000683.1:g.19179271C>G	GRCh37
NC_000021.7:g.18101142C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284881.9:c.128-9836G>C MANE Select	ENSP00000284881.4:n.128-9836G>C
ENST00000284881.8:c.128-9836G>C	ENSP00000284881.4:n.128-9836G>C
ENST00000400558.7:c.128-9836G>C	ENSP00000383403.3:n.128-9836G>C
ENST00000400559.7:c.128-9836G>C	ENSP00000383404.3:n.128-9836G>C
ENST00000405964.2:c.128-9836G>C	ENSP00000385566.2:n.128-9836G>C
ENST00000493464.1:n.348+4402G>C
NM_001100420.1:c.128-9836G>C	NP_001093890.1:n.128-9836G>C
NM_001100421.1:c.128-9836G>C	NP_001093891.1:n.128-9836G>C
NM_017447.3:c.128-9836G>C	NP_059143.3:n.128-9836G>C
XR_937601.1:n.449+3078C>G
NM_001100420.2:c.128-9836G>C MANE Select	NP_001093890.1:n.128-9836G>C
NM_001100421.2:c.128-9836G>C	NP_001093891.1:n.128-9836G>C
NM_017447.4:c.128-9836G>C	NP_059143.3:n.128-9836G>C