Canonical Allele Identifier: CA1845635724

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647221A= , CM000671.2:g.34647221A=	GRCh38
NC_000009.11:g.34647218A= , CM000671.1:g.34647218A=	GRCh37
NC_000009.10:g.34637218A=	NCBI36
NG_009029.1:g.5584A=
NG_028966.1:g.37A=
NG_009029.2:g.5633A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.215A=	ENSP00000509954.1:p.Asn72=
ENST00000378842.8:c.215A= MANE Select	ENSP00000368119.4:p.Asn72=
ENST00000378842.7:c.215A=	ENSP00000368119.3:p.Asn72=
ENST00000450095.6:c.13A=	ENSP00000401956.2:p.Thr5=
ENST00000465543.6:n.554A=
ENST00000468099.2:n.255A=
ENST00000472111.5:n.256A=
ENST00000473506.6:c.215A=	ENSP00000432839.2:p.Asn72=
ENST00000473529.5:n.262A=
ENST00000485531.1:n.208A=
ENST00000487381.5:n.241A=
ENST00000489643.6:n.245A=
ENST00000554085.5:c.215A=	ENSP00000450419.1:p.Asn72=
ENST00000554139.5:n.268A=
ENST00000554330.5:n.212A=
ENST00000554550.5:c.215A=	ENSP00000451435.1:p.Asn72=
ENST00000554638.5:n.239A=
ENST00000554897.5:c.215A=	ENSP00000450942.1:p.Asn72=
ENST00000554944.5:n.245A=
ENST00000555020.5:n.245A=
ENST00000555086.5:n.219A=
ENST00000555214.5:n.224A=
ENST00000556157.1:n.322A=
ENST00000556244.1:c.99A=
ENST00000556278.1:c.215A=	ENSP00000451792.1:p.Asn72=
ENST00000556403.5:n.228A=
ENST00000556494.5:n.247A=
ENST00000557541.5:n.408A=
ENST00000557706.5:n.329A=
NM_000155.3:c.215A=	NP_000146.2:p.Asn72=
NM_001258332.1:c.13A=	NP_001245261.1:p.Thr5=
NM_000155.4:c.215A= MANE Select	NP_000146.2:p.Asn72=
NM_001258332.2:c.13A=	NP_001245261.1:p.Thr5=