Canonical Allele Identifier: CA2153356432

Gene: GALC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87945534T= , CM000676.2:g.87945534T=	GRCh38
NC_000014.8:g.88411878T= , CM000676.1:g.88411878T=	GRCh37
NC_000014.7:g.87481631T=	NCBI36
NG_011853.2:g.53030A=
NG_011853.3:g.53030A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1670+19A= MANE Select	ENSP00000261304.2:n.1670+19A=
ENST00000261304.6:c.1670+19A=	ENSP00000261304.2:n.1670+19A=
ENST00000393568.8:c.1601+19A=	ENSP00000377198.4:n.1601+19A=
ENST00000393569.6:c.1592+19A=	ENSP00000377199.2:n.1592+19A=
ENST00000544807.6:c.1502+19A=	ENSP00000437513.2:n.1502+19A=
ENST00000555000.5:c.1037+19A=	ENSP00000450472.1:n.1037+19A=
ENST00000555179.1:c.206+2194A=
ENST00000557316.5:c.*1068+19A=	ENSP00000452314.1:n.*1068+19A=
NM_000153.3:c.1670+19A=	NP_000144.2:n.1670+19A=
NM_001201401.1:c.1601+19A=	NP_001188330.1:n.1601+19A=
NM_001201402.1:c.1592+19A=	NP_001188331.1:n.1592+19A=
XM_011536618.1:c.1502+19A=	XP_011534920.1:n.1502+19A=
XM_011536618.2:c.1502+19A=	XP_011534920.1:n.1502+19A=
NM_000153.4:c.1670+19A= MANE Select	NP_000144.2:n.1670+19A=
NM_001201401.2:c.1601+19A=	NP_001188330.1:n.1601+19A=
NM_001201402.2:c.1592+19A=	NP_001188331.1:n.1592+19A=