Canonical Allele Identifier: CA6845123

Gene: CLIP1

Linked Data

• ClinVar Variation Id: 434777
• ClinVar RCV Id: RCV000499475
• dbSNP Id: rs368149044
• ExAC: 12:122812484 C / T
• gnomAD v2: 12-122812484-C-T
• gnomAD v3: 12-122327937-C-T
• gnomAD v4: 12-122327937-C-T
• COSMIC: COSM299136
• MyVariant Identifiers: chr12:g.122812484C>T (hg19) ; chr12:g.122327937C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.122327937C>T , CM000674.2:g.122327937C>T	GRCh38
NC_000012.11:g.122812484C>T , CM000674.1:g.122812484C>T	GRCh37
NC_000012.10:g.121378437C>T	NCBI36
NG_030352.1:g.99633G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537123.2:c.216+10G>A	ENSP00000497285.1:n.216+10G>A
ENST00000545889.6:c.2124+10G>A	ENSP00000438743.2:n.2124+10G>A
ENST00000620786.5:c.3249+10G>A MANE Select	ENSP00000479322.1:n.3249+10G>A
ENST00000648993.1:c.1302+10G>A	ENSP00000497665.1:n.1302+10G>A
ENST00000302528.11:c.3216+10G>A	ENSP00000303585.7:n.3216+10G>A
ENST00000358808.6:c.3216+10G>A	ENSP00000351665.2:n.3216+10G>A
ENST00000361654.8:c.2883+10G>A	ENSP00000355314.4:n.2883+10G>A
ENST00000537178.5:c.3111+10G>A	ENSP00000445531.1:n.3111+10G>A
ENST00000540338.5:c.3249+10G>A	ENSP00000439093.1:n.3249+10G>A
ENST00000545889.5:c.1974+10G>A	ENSP00000438743.1:n.1974+10G>A
ENST00000620786.4:c.3249+10G>A	ENSP00000479322.1:n.3249+10G>A
NM_001247997.1:c.3249+10G>A	NP_001234926.1:n.3249+10G>A
NM_002956.2:c.3216+10G>A	NP_002947.1:n.3216+10G>A
NM_198240.1:c.3111+10G>A	NP_937883.1:n.3111+10G>A
XM_005253593.2:c.3249+10G>A	XP_005253650.1:n.3249+10G>A
XM_006719552.2:c.3216+10G>A	XP_006719615.1:n.3216+10G>A
XM_005253593.3:c.3249+10G>A	XP_005253650.1:n.3249+10G>A
XM_006719552.4:c.3216+10G>A	XP_006719615.1:n.3216+10G>A
XM_017019786.1:c.3216+10G>A	XP_016875275.1:n.3216+10G>A
XM_017019787.2:c.3132+10G>A	XP_016875276.1:n.3132+10G>A
XM_017019788.2:c.3111+10G>A	XP_016875277.1:n.3111+10G>A
XM_017019789.1:c.3111+10G>A	XP_016875278.1:n.3111+10G>A
XM_017019790.1:c.3111+10G>A	XP_016875279.1:n.3111+10G>A
XM_017019791.2:c.3099+10G>A	XP_016875280.1:n.3099+10G>A
XM_017019792.2:c.2994+10G>A	XP_016875281.1:n.2994+10G>A
NM_198240.2:c.3111+10G>A	NP_937883.1:n.3111+10G>A
NM_001247997.2:c.3249+10G>A MANE Select	NP_001234926.1:n.3249+10G>A
NM_001389291.1:c.3111+10G>A	NP_001376220.1:n.3111+10G>A
NM_002956.3:c.3216+10G>A	NP_002947.1:n.3216+10G>A
NM_198240.3:c.3111+10G>A	NP_937883.1:n.3111+10G>A