Canonical Allele Identifier: CA2010386

Gene: CERKL ITGA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181538249A>T , CM000664.2:g.181538249A>T	GRCh38
NC_000002.11:g.182402976A>T , CM000664.1:g.182402976A>T	GRCh37
NC_000002.10:g.182111221A>T	NCBI36
NG_021178.1:g.123859T>A
NG_050623.1:g.86358A>T
NG_021178.2:g.123859T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000885.6:c.*2722A>T (ITGA4) MANE Select	NP_000876.3:n.*2722A>T
NM_201548.5:c.1539-5T>A (CERKL) MANE Select	NP_963842.1:n.1539-5T>A
ENST00000397033.7:c.*2722A>T (ITGA4) MANE Select	ENSP00000380227.2:n.*2722A>T
ENST00000410087.8:c.1539-5T>A (CERKL) MANE Select	ENSP00000386725.3:n.1539-5T>A
NM_000885.5:c.*2722A>T (ITGA4)	NP_000876.3:n.*2722A>T
NM_001030311.2:c.1617-5T>A (CERKL)	NP_001025482.1:n.1617-5T>A
NM_001030311.3:c.1617-5T>A (CERKL)	NP_001025482.1:n.1617-5T>A
NM_001030312.2:c.1200-5T>A (CERKL)	NP_001025483.1:n.1200-5T>A
NM_001030312.3:c.1200-5T>A (CERKL)	NP_001025483.1:n.1200-5T>A
NM_001030313.2:c.1332-5T>A (CERKL)	NP_001025484.1:n.1332-5T>A
NM_001030313.3:c.1332-5T>A (CERKL)	NP_001025484.1:n.1332-5T>A
NM_001160277.1:c.1485-5T>A (CERKL)	NP_001153749.1:n.1485-5T>A
NM_001160277.2:c.1485-5T>A (CERKL)	NP_001153749.1:n.1485-5T>A
NM_201548.4:c.1539-5T>A (CERKL)	NP_963842.1:n.1539-5T>A
NR_027689.1:n.1444-5T>A (CERKL)
NR_027689.2:n.1442-5T>A (CERKL)
NR_027690.1:n.1576-5T>A (CERKL)
NR_027690.2:n.1574-5T>A (CERKL)
ENST00000339098.9:c.1617-5T>A (CERKL)	ENSP00000341159.5:n.1617-5T>A
ENST00000374967.6:c.1475-5T>A (CERKL)	ENSP00000364106.2:n.1475-5T>A
ENST00000374969.6:c.1200-5T>A (CERKL)	ENSP00000364108.2:n.1200-5T>A
ENST00000374970.6:c.1332-5T>A (CERKL)	ENSP00000364109.2:n.1332-5T>A
ENST00000409440.7:c.1485-5T>A (CERKL)	ENSP00000387080.3:n.1485-5T>A
ENST00000410087.7:c.1539-5T>A (CERKL)	ENSP00000386725.3:n.1539-5T>A
ENST00000421817.5:c.*795-5T>A (CERKL)	ENSP00000411466.1:n.*795-5T>A
ENST00000452174.5:c.1343-5T>A (CERKL)	ENSP00000409198.1:n.1343-5T>A
ENST00000494398.5:n.2331-5T>A (CERKL)
ENST00000684145.1:c.783-5T>A (CERKL)	ENSP00000508396.1:n.783-5T>A