Canonical Allele Identifier: CA464403169

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648842C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648845C>T , CM000671.2:g.34648845C>T	GRCh38
NC_000009.11:g.34648842C>T , CM000671.1:g.34648842C>T	GRCh37
NC_000009.10:g.34638842C>T	NCBI36
NG_009029.1:g.7208C>T
NG_028966.1:g.1661C>T
NG_009029.2:g.7257C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*359C>T	ENSP00000509954.1:n.*359C>T
ENST00000378842.8:c.771C>T MANE Select	ENSP00000368119.4:p.Pro257=
ENST00000378842.7:c.771C>T	ENSP00000368119.3:p.Pro257=
ENST00000450095.6:c.444C>T	ENSP00000401956.2:p.Pro148=
ENST00000473506.6:c.*359C>T	ENSP00000432839.2:n.*359C>T
ENST00000489643.6:n.851C>T
ENST00000554085.5:c.*515C>T	ENSP00000450419.1:n.*515C>T
ENST00000554550.5:c.*391C>T	ENSP00000451435.1:n.*391C>T
ENST00000554638.5:n.1243C>T
ENST00000555020.5:n.1232C>T
ENST00000555086.5:n.775C>T
ENST00000555754.1:n.116C>T
ENST00000556244.1:c.758C>T
ENST00000556278.1:c.432+389C>T	ENSP00000451792.1:n.432+389C>T
ENST00000557706.5:n.1333C>T
NM_000155.3:c.771C>T	NP_000146.2:p.Pro257=
NM_001258332.1:c.444C>T	NP_001245261.1:p.Pro148=
NM_000155.4:c.771C>T MANE Select	NP_000146.2:p.Pro257=
NM_001258332.2:c.444C>T	NP_001245261.1:p.Pro148=