Canonical Allele Identifier: CA1807098168

Gene: BAALC BAALC-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.103141321G= , CM000670.2:g.103141321G=	GRCh38
NC_000008.10:g.104153549G= , CM000670.1:g.104153549G=	GRCh37
NC_000008.9:g.104222725G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309982.10:c.160+264G= (BAALC) MANE Select	ENSP00000312457.5:n.160+264G=
ENST00000297574.6:c.160+264G= (BAALC)	ENSP00000297574.6:n.160+264G=
ENST00000306391.10:c.160+264G= (BAALC)	ENSP00000302559.6:n.160+264G=
ENST00000309982.9:c.160+264G= (BAALC)	ENSP00000312457.5:n.160+264G=
ENST00000330955.5:c.160+264G= (BAALC)	ENSP00000331579.5:n.160+264G=
ENST00000438105.2:c.160+264G= (BAALC)	ENSP00000395024.2:n.160+264G=
NM_001024372.1:c.160+264G= (BAALC)	NP_001019543.1:n.160+264G=
NM_024812.2:c.160+264G= (BAALC)	NP_079088.1:n.160+264G=
NR_027071.1:n.22C= (BAALC-AS2)
NM_001364874.1:c.160+264G= (BAALC)	NP_001351803.1:n.160+264G=
XR_001745601.2:n.310+264G= (BAALC)
NM_024812.3:c.160+264G= (BAALC) MANE Select	NP_079088.1:n.160+264G=
NM_001024372.2:c.160+264G= (BAALC)	NP_001019543.1:n.160+264G=