Canonical Allele Identifier: CA2581090705

Gene: CALCOCO1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53720374C>A , CM000674.2:g.53720374C>A	GRCh38
NC_000012.11:g.54114158C>A , CM000674.1:g.54114158C>A	GRCh37
NC_000012.10:g.52400425C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020898.3:c.759-545G>T MANE Select	NP_065949.1:n.759-545G>T
ENST00000550804.6:c.759-545G>T MANE Select	ENSP00000449960.1:n.759-545G>T
NM_001143682.1:c.660-545G>T	NP_001137154.1:n.660-545G>T
NM_001143682.2:c.660-545G>T	NP_001137154.1:n.660-545G>T
NM_020898.2:c.759-545G>T	NP_065949.1:n.759-545G>T
NR_026554.1:n.800-545G>T
NR_026554.2:n.729-545G>T
ENST00000262059.8:c.759-545G>T	ENSP00000262059.4:n.759-545G>T
ENST00000430117.6:c.660-545G>T	ENSP00000397189.2:n.660-545G>T
ENST00000547988.5:n.1220-545G>T
ENST00000548263.5:c.759-545G>T	ENSP00000447647.1:n.759-545G>T
ENST00000549935.6:n.811-545G>T
ENST00000550804.5:c.759-545G>T	ENSP00000449960.1:n.759-545G>T
XM_011538601.1:c.759-545G>T	XP_011536903.1:n.759-545G>T
XM_011538602.1:c.759-545G>T	XP_011536904.1:n.759-545G>T
XM_011538603.1:c.759-545G>T	XP_011536905.1:n.759-545G>T
XM_011538603.2:c.759-545G>T	XP_011536905.1:n.759-545G>T
XM_011538604.1:c.759-545G>T	XP_011536906.1:n.759-545G>T
XM_011538604.2:c.759-545G>T	XP_011536906.1:n.759-545G>T
XM_017019707.1:c.759-545G>T	XP_016875196.1:n.759-545G>T
XM_017019708.2:c.-393-363G>T	XP_016875197.1:n.-393-363G>T
XM_017019709.2:c.-393-363G>T	XP_016875198.1:n.-393-363G>T