Canonical Allele Identifier: CA2839349899

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649374G>T , CM000671.2:g.34649374G>T	GRCh38
NC_000009.11:g.34649371G>T , CM000671.1:g.34649371G>T	GRCh37
NC_000009.10:g.34639371G>T	NCBI36
NG_009029.1:g.7737G>T
NG_028966.1:g.2190G>T
NG_009029.2:g.7786G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*493-36G>T	ENSP00000509954.1:n.*493-36G>T
ENST00000378842.8:c.905-36G>T MANE Select	ENSP00000368119.4:n.905-36G>T
ENST00000378842.7:c.905-36G>T	ENSP00000368119.3:n.905-36G>T
ENST00000450095.6:c.578-36G>T	ENSP00000401956.2:n.578-36G>T
ENST00000488412.2:n.453G>T
ENST00000489643.6:n.1277G>T
ENST00000554550.5:c.*525-36G>T	ENSP00000451435.1:n.*525-36G>T
ENST00000554638.5:n.1377-36G>T
ENST00000555020.5:n.1658G>T
ENST00000555754.1:n.353-36G>T
ENST00000556278.1:c.432+918G>T	ENSP00000451792.1:n.432+918G>T
ENST00000557706.5:n.1480-36G>T
NM_000155.3:c.905-36G>T	NP_000146.2:n.905-36G>T
NM_001258332.1:c.578-36G>T	NP_001245261.1:n.578-36G>T
NM_000155.4:c.905-36G>T MANE Select	NP_000146.2:n.905-36G>T
NM_001258332.2:c.578-36G>T	NP_001245261.1:n.578-36G>T