Canonical Allele Identifier: CA10612122

Gene: CERKL ITGA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181538092C>G , CM000664.2:g.181538092C>G	GRCh38
NC_000002.11:g.182402819C>G , CM000664.1:g.182402819C>G	GRCh37
NC_000002.10:g.182111064C>G	NCBI36
NG_021178.1:g.124016G>C
NG_050623.1:g.86201C>G
NG_021178.2:g.124016G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000885.6:c.*2565C>G (ITGA4) MANE Select	NP_000876.3:n.*2565C>G
NM_201548.5:c.*92G>C (CERKL) MANE Select	NP_963842.1:n.*92G>C
ENST00000397033.7:c.*2565C>G (ITGA4) MANE Select	ENSP00000380227.2:n.*2565C>G
ENST00000410087.8:c.*92G>C (CERKL) MANE Select	ENSP00000386725.3:n.*92G>C
NM_000885.5:c.*2565C>G (ITGA4)	NP_000876.3:n.*2565C>G
NM_001030311.2:c.*92G>C (CERKL)	NP_001025482.1:n.*92G>C
NM_001030311.3:c.*92G>C (CERKL)	NP_001025482.1:n.*92G>C
NM_001030312.2:c.*92G>C (CERKL)	NP_001025483.1:n.*92G>C
NM_001030312.3:c.*92G>C (CERKL)	NP_001025483.1:n.*92G>C
NM_001030313.2:c.*92G>C (CERKL)	NP_001025484.1:n.*92G>C
NM_001030313.3:c.*92G>C (CERKL)	NP_001025484.1:n.*92G>C
NM_001160277.1:c.*92G>C (CERKL)	NP_001153749.1:n.*92G>C
NM_001160277.2:c.*92G>C (CERKL)	NP_001153749.1:n.*92G>C
NM_201548.4:c.*92G>C (CERKL)	NP_963842.1:n.*92G>C
NR_027689.1:n.1596G>C (CERKL)
NR_027689.2:n.1594G>C (CERKL)
NR_027690.1:n.1728G>C (CERKL)
NR_027690.2:n.1726G>C (CERKL)
ENST00000409440.7:c.*92G>C (CERKL)	ENSP00000387080.3:n.*92G>C
ENST00000410087.7:c.*92G>C (CERKL)	ENSP00000386725.3:n.*92G>C
ENST00000684145.1:c.*92G>C (CERKL)	ENSP00000508396.1:n.*92G>C