Canonical Allele Identifier: CA428553868

Gene: CKAP2L

Linked Data

• MyVariant Identifiers: chr2:g.113514267C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756690C>T , CM000664.2:g.112756690C>T	GRCh38
NC_000002.11:g.113514267C>T , CM000664.1:g.113514267C>T	GRCh37
NC_000002.10:g.113230738C>T	NCBI36
NG_041820.1:g.12988G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.681G>A MANE Select	ENSP00000305204.6:p.Leu227=
ENST00000302450.10:c.681G>A	ENSP00000305204.6:p.Leu227=
ENST00000435431.5:c.478+203G>A	ENSP00000414834.1:n.478+203G>A
NM_001304361.1:c.186G>A	NP_001291290.1:p.Leu62=
NM_152515.4:c.681G>A	NP_689728.3:p.Leu227=
NR_130712.1:n.557+203G>A
XM_011510666.1:c.186G>A	XP_011508968.1:p.Leu62=
XM_011510666.2:c.186G>A	XP_011508968.1:p.Leu62=
NM_152515.5:c.681G>A MANE Select	NP_689728.3:p.Leu227=
NM_001304361.2:c.186G>A	NP_001291290.1:p.Leu62=
NR_130712.2:n.489+203G>A