Canonical Allele Identifier: CA373279109

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647502A>C (hg19) ; chr9:g.34647505A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647505A>C , CM000671.2:g.34647505A>C	GRCh38
NC_000009.11:g.34647502A>C , CM000671.1:g.34647502A>C	GRCh37
NC_000009.10:g.34637502A>C	NCBI36
NG_009029.1:g.5868A>C
NG_028966.1:g.321A>C
NG_009029.2:g.5917A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.266A>C	ENSP00000509954.1:p.Tyr89Ser
ENST00000378842.8:c.266A>C MANE Select	ENSP00000368119.4:p.Tyr89Ser
ENST00000378842.7:c.266A>C	ENSP00000368119.3:p.Tyr89Ser
ENST00000450095.6:c.50+247A>C	ENSP00000401956.2:n.50+247A>C
ENST00000465543.6:n.605A>C
ENST00000468099.2:n.539A>C
ENST00000472111.5:n.307A>C
ENST00000473506.6:c.253-36A>C	ENSP00000432839.2:n.253-36A>C
ENST00000473529.5:n.313A>C
ENST00000485531.1:n.492A>C
ENST00000487381.5:n.525A>C
ENST00000489643.6:n.282+247A>C
ENST00000554085.5:c.*10A>C	ENSP00000450419.1:n.*10A>C
ENST00000554139.5:n.319A>C
ENST00000554330.5:n.250-36A>C
ENST00000554550.5:c.252+247A>C	ENSP00000451435.1:n.252+247A>C
ENST00000554638.5:n.523A>C
ENST00000554897.5:c.252+247A>C	ENSP00000450942.1:n.252+247A>C
ENST00000554944.5:n.283-36A>C
ENST00000555020.5:n.296A>C
ENST00000555086.5:n.270A>C
ENST00000555214.5:n.261+247A>C
ENST00000556157.1:n.390A>C
ENST00000556244.1:c.253A>C
ENST00000556278.1:c.252+247A>C	ENSP00000451792.1:n.252+247A>C
ENST00000556403.5:n.279A>C
ENST00000556494.5:n.298A>C
ENST00000557541.5:n.446-36A>C
ENST00000557706.5:n.613A>C
NM_000155.3:c.266A>C	NP_000146.2:p.Tyr89Ser
NM_001258332.1:c.50+247A>C	NP_001245261.1:n.50+247A>C
NM_000155.4:c.266A>C MANE Select	NP_000146.2:p.Tyr89Ser
NM_001258332.2:c.50+247A>C	NP_001245261.1:n.50+247A>C