Canonical Allele Identifier: CA373284793

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34649443A>C (hg19) ; chr9:g.34649446A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649446A>C , CM000671.2:g.34649446A>C	GRCh38
NC_000009.11:g.34649443A>C , CM000671.1:g.34649443A>C	GRCh37
NC_000009.10:g.34639443A>C	NCBI36
NG_009029.1:g.7809A>C
NG_028966.1:g.2262A>C
NG_009029.2:g.7858A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*529A>C	ENSP00000509954.1:n.*529A>C
ENST00000378842.8:c.941A>C MANE Select	ENSP00000368119.4:p.Asn314Thr
ENST00000378842.7:c.941A>C	ENSP00000368119.3:p.Asn314Thr
ENST00000450095.6:c.614A>C	ENSP00000401956.2:p.Asn205Thr
ENST00000488412.2:n.525A>C
ENST00000489643.6:n.1349A>C
ENST00000554550.5:c.*561A>C	ENSP00000451435.1:n.*561A>C
ENST00000554638.5:n.1413A>C
ENST00000555020.5:n.1730A>C
ENST00000555754.1:n.389A>C
ENST00000556278.1:c.432+990A>C	ENSP00000451792.1:n.432+990A>C
ENST00000557706.5:n.1516A>C
NM_000155.3:c.941A>C	NP_000146.2:p.Asn314Thr
NM_001258332.1:c.614A>C	NP_001245261.1:p.Asn205Thr
NM_000155.4:c.941A>C MANE Select	NP_000146.2:p.Asn314Thr
NM_001258332.2:c.614A>C	NP_001245261.1:p.Asn205Thr