Canonical Allele Identifier: CA2964907

Gene: ODAPH

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.75556520C>A , CM000666.2:g.75556520C>A	GRCh38
NC_000004.11:g.76481730C>A , CM000666.1:g.76481730C>A	GRCh37
NC_000004.10:g.76700754C>A	NCBI36
NG_032974.1:g.5473C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311623.9:c.67+371C>A MANE Select	ENSP00000311307.5:n.67+371C>A
ENST00000311623.8:c.67+371C>A	ENSP00000311307.4:n.67+371C>A
ENST00000435974.2:c.68-21C>A	ENSP00000406925.2:n.68-21C>A
ENST00000511093.5:c.67+371C>A	ENSP00000421429.1:n.67+371C>A
ENST00000514064.1:n.103-21C>A
ENST00000616557.1:c.67+371C>A	ENSP00000479147.1:n.67+371C>A
NM_001206981.1:c.68-21C>A	NP_001193910.1:n.68-21C>A
NM_001257072.1:c.67+371C>A	NP_001244001.1:n.67+371C>A
NM_178497.3:c.67+371C>A	NP_848592.2:n.67+371C>A
NR_046429.1:n.103-21C>A
NR_046430.1:n.102+371C>A
XM_011531668.1:c.68-21C>A	XP_011529970.1:n.68-21C>A
XM_011531668.2:c.68-21C>A	XP_011529970.1:n.68-21C>A
NM_001206981.2:c.68-21C>A	NP_001193910.1:n.68-21C>A
NM_178497.5:c.67+371C>A MANE Select	NP_848592.2:n.67+371C>A
NR_046429.2:n.85-21C>A
NR_046430.2:n.84+371C>A
NM_001257072.2:c.67+371C>A	NP_001244001.1:n.67+371C>A
NR_046429.3:n.85-21C>A
NR_046430.3:n.84+371C>A