Canonical Allele Identifier: CA2520670238

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648931_34648932dup , CM000671.2:g.34648931_34648932dup	GRCh38
NC_000009.11:g.34648928_34648929dup , CM000671.1:g.34648928_34648929dup	GRCh37
NC_000009.10:g.34638928_34638929dup	NCBI36
NG_009029.1:g.7294_7295dup
NG_028966.1:g.1747_1748dup
NG_009029.2:g.7343_7344dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*408+37_*408+38dup	ENSP00000509954.1:n.*408+37_*408+38dup
ENST00000378842.8:c.820+37_820+38dup MANE Select	ENSP00000368119.4:n.820+37_820+38dup
ENST00000378842.7:c.820+37_820+38dup	ENSP00000368119.3:n.820+37_820+38dup
ENST00000450095.6:c.493+37_493+38dup	ENSP00000401956.2:n.493+37_493+38dup
ENST00000488412.2:n.10_11dup
ENST00000489643.6:n.900+37_900+38dup
ENST00000554085.5:c.*564+37_*564+38dup	ENSP00000450419.1:n.*564+37_*564+38dup
ENST00000554550.5:c.*440+37_*440+38dup	ENSP00000451435.1:n.*440+37_*440+38dup
ENST00000554638.5:n.1292+37_1292+38dup
ENST00000555020.5:n.1281+37_1281+38dup
ENST00000555086.5:n.861_862dup
ENST00000555754.1:n.202_203dup
ENST00000556278.1:c.432+475_432+476dup	ENSP00000451792.1:n.432+475_432+476dup
ENST00000557706.5:n.1395+24_1395+25dup
NM_000155.3:c.820+37_820+38dup	NP_000146.2:n.820+37_820+38dup
NM_001258332.1:c.493+37_493+38dup	NP_001245261.1:n.493+37_493+38dup
NM_000155.4:c.820+37_820+38dup MANE Select	NP_000146.2:n.820+37_820+38dup
NM_001258332.2:c.493+37_493+38dup	NP_001245261.1:n.493+37_493+38dup