Canonical Allele Identifier: CA2841055845

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649350G>C , CM000671.2:g.34649350G>C	GRCh38
NC_000009.11:g.34649347G>C , CM000671.1:g.34649347G>C	GRCh37
NC_000009.10:g.34639347G>C	NCBI36
NG_009029.1:g.7713G>C
NG_028966.1:g.2166G>C
NG_009029.2:g.7762G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*493-60G>C	ENSP00000509954.1:n.*493-60G>C
ENST00000378842.8:c.905-60G>C MANE Select	ENSP00000368119.4:n.905-60G>C
ENST00000378842.7:c.905-60G>C	ENSP00000368119.3:n.905-60G>C
ENST00000450095.6:c.578-60G>C	ENSP00000401956.2:n.578-60G>C
ENST00000488412.2:n.429G>C
ENST00000489643.6:n.1253G>C
ENST00000554550.5:c.*525-60G>C	ENSP00000451435.1:n.*525-60G>C
ENST00000554638.5:n.1377-60G>C
ENST00000555020.5:n.1634G>C
ENST00000555754.1:n.353-60G>C
ENST00000556278.1:c.432+894G>C	ENSP00000451792.1:n.432+894G>C
ENST00000557706.5:n.1480-60G>C
NM_000155.3:c.905-60G>C	NP_000146.2:n.905-60G>C
NM_001258332.1:c.578-60G>C	NP_001245261.1:n.578-60G>C
NM_000155.4:c.905-60G>C MANE Select	NP_000146.2:n.905-60G>C
NM_001258332.2:c.578-60G>C	NP_001245261.1:n.578-60G>C