Canonical Allele Identifier: CA373281276

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648111G>T (hg19) ; chr9:g.34648114G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648114G>T , CM000671.2:g.34648114G>T	GRCh38
NC_000009.11:g.34648111G>T , CM000671.1:g.34648111G>T	GRCh37
NC_000009.10:g.34638111G>T	NCBI36
NG_009029.1:g.6477G>T
NG_028966.1:g.930G>T
NG_009029.2:g.6526G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*96-1G>T	ENSP00000509954.1:n.*96-1G>T
ENST00000378842.8:c.508-1G>T MANE Select	ENSP00000368119.4:n.508-1G>T
ENST00000378842.7:c.508-1G>T	ENSP00000368119.3:n.508-1G>T
ENST00000450095.6:c.181-1G>T	ENSP00000401956.2:n.181-1G>T
ENST00000465543.6:n.847-1G>T
ENST00000472111.5:n.764-1G>T
ENST00000473506.6:c.*96-1G>T	ENSP00000432839.2:n.*96-1G>T
ENST00000473529.5:n.666G>T
ENST00000485531.1:n.1101G>T
ENST00000487381.5:n.893-1G>T
ENST00000489643.6:n.283-1G>T
ENST00000554085.5:c.*252-1G>T	ENSP00000450419.1:n.*252-1G>T
ENST00000554139.5:n.753G>T
ENST00000554550.5:c.*128-1G>T	ENSP00000451435.1:n.*128-1G>T
ENST00000554638.5:n.980-1G>T
ENST00000554897.5:c.*194G>T	ENSP00000450942.1:n.*194G>T
ENST00000554944.5:n.856G>T
ENST00000555020.5:n.664-1G>T
ENST00000555086.5:n.512-1G>T
ENST00000555214.5:n.328G>T
ENST00000556244.1:c.495-1G>T
ENST00000556278.1:c.253-1G>T	ENSP00000451792.1:n.253-1G>T
ENST00000556494.5:n.629-1G>T
ENST00000557706.5:n.1070-1G>T
NM_000155.3:c.508-1G>T	NP_000146.2:n.508-1G>T
NM_001258332.1:c.181-1G>T	NP_001245261.1:n.181-1G>T
NM_000155.4:c.508-1G>T MANE Select	NP_000146.2:n.508-1G>T
NM_001258332.2:c.181-1G>T	NP_001245261.1:n.181-1G>T