Canonical Allele Identifier: CA1836798

Gene: CKAP2L

Linked Data

• dbSNP Id: rs768009129
• ExAC: 2:113514195 G / A
• gnomAD v2: 2-113514195-G-A
• gnomAD v4: 2-112756618-G-A
• MyVariant Identifiers: chr2:g.113514195G>A (hg19) ; chr2:g.112756618G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756618G>A , CM000664.2:g.112756618G>A	GRCh38
NC_000002.11:g.113514195G>A , CM000664.1:g.113514195G>A	GRCh37
NC_000002.10:g.113230666G>A	NCBI36
NG_041820.1:g.13060C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.753C>T MANE Select	ENSP00000305204.6:p.Ser251=
ENST00000302450.10:c.753C>T	ENSP00000305204.6:p.Ser251=
ENST00000435431.5:c.478+275C>T	ENSP00000414834.1:n.478+275C>T
NM_001304361.1:c.258C>T	NP_001291290.1:p.Ser86=
NM_152515.4:c.753C>T	NP_689728.3:p.Ser251=
NR_130712.1:n.557+275C>T
XM_011510666.1:c.258C>T	XP_011508968.1:p.Ser86=
XM_011510666.2:c.258C>T	XP_011508968.1:p.Ser86=
NM_152515.5:c.753C>T MANE Select	NP_689728.3:p.Ser251=
NM_001304361.2:c.258C>T	NP_001291290.1:p.Ser86=
NR_130712.2:n.489+275C>T