Canonical Allele Identifier: CA373285265

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34649543G>T (hg19) ; chr9:g.34649546G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649546G>T , CM000671.2:g.34649546G>T	GRCh38
NC_000009.11:g.34649543G>T , CM000671.1:g.34649543G>T	GRCh37
NC_000009.10:g.34639543G>T	NCBI36
NG_009029.1:g.7909G>T
NG_028966.1:g.2362G>T
NG_009029.2:g.7958G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*629G>T	ENSP00000509954.1:n.*629G>T
ENST00000378842.8:c.1041G>T MANE Select	ENSP00000368119.4:p.Arg347Ser
ENST00000378842.7:c.1041G>T	ENSP00000368119.3:p.Arg347Ser
ENST00000450095.6:c.714G>T	ENSP00000401956.2:p.Arg238Ser
ENST00000488412.2:n.625G>T
ENST00000489643.6:n.1449G>T
ENST00000554550.5:c.*661G>T	ENSP00000451435.1:n.*661G>T
ENST00000554638.5:n.1513G>T
ENST00000555020.5:n.1830G>T
ENST00000555754.1:n.489G>T
ENST00000556278.1:c.432+1090G>T	ENSP00000451792.1:n.432+1090G>T
ENST00000557706.5:n.1616G>T
NM_000155.3:c.1041G>T	NP_000146.2:p.Arg347Ser
NM_001258332.1:c.714G>T	NP_001245261.1:p.Arg238Ser
NM_000155.4:c.1041G>T MANE Select	NP_000146.2:p.Arg347Ser
NM_001258332.2:c.714G>T	NP_001245261.1:p.Arg238Ser