Canonical Allele Identifier: CA13809375

Gene: SOHLH2 CCDC169-SOHLH2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.36196880C>T , CM000675.2:g.36196880C>T	GRCh38
NC_000013.10:g.36771017C>T , CM000675.1:g.36771017C>T	GRCh37
NC_000013.9:g.35669017C>T	NCBI36
NG_033786.1:g.22736G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379881.8:c.264-3013G>A (SOHLH2) MANE Select	ENSP00000369210.3:n.264-3013G>A
ENST00000317764.6:c.264-3013G>A (SOHLH2)	ENSP00000326838.6:n.264-3013G>A
ENST00000379881.7:c.264-3013G>A (SOHLH2)	ENSP00000369210.3:n.264-3013G>A
ENST00000511166.1:c.495-3013G>A (CCDC169-SOHLH2)	ENSP00000421868.1:n.495-3013G>A
NM_001198910.1:c.495-3013G>A (CCDC169-SOHLH2)	NP_001185839.1:n.495-3013G>A
NM_001282147.1:c.264-3013G>A (SOHLH2)	NP_001269076.1:n.264-3013G>A
NM_017826.2:c.264-3013G>A (SOHLH2)	NP_060296.2:n.264-3013G>A
NM_017826.3:c.264-3013G>A (SOHLH2) MANE Select	NP_060296.2:n.264-3013G>A
NM_001198910.2:c.495-3013G>A (CCDC169-SOHLH2)	NP_001185839.1:n.495-3013G>A
NM_001282147.2:c.264-3013G>A (SOHLH2)	NP_001269076.1:n.264-3013G>A