Canonical Allele Identifier: CA1845641168

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649453_34649454delinsGC , CM000671.2:g.34649453_34649454delinsGC	GRCh38
NC_000009.11:g.34649450_34649451delinsGC , CM000671.1:g.34649450_34649451delinsGC	GRCh37
NC_000009.10:g.34639450_34639451delinsGC	NCBI36
NG_009029.1:g.7816_7817delinsGC
NG_028966.1:g.2269_2270delinsGC
NG_009029.2:g.7865_7866delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*536_*537delinsGC	ENSP00000509954.1:n.*536_*537delinsGC
ENST00000378842.8:c.948_949delinsGC MANE Select	ENSP00000368119.4:p.Trp316=
ENST00000378842.7:c.948_949delinsGC	ENSP00000368119.3:p.Trp316=
ENST00000450095.6:c.621_622delinsGC	ENSP00000401956.2:p.Trp207=
ENST00000488412.2:n.532_533delinsGC
ENST00000489643.6:n.1356_1357delinsGC
ENST00000554550.5:c.*568_*569delinsGC	ENSP00000451435.1:n.*568_*569delinsGC
ENST00000554638.5:n.1420_1421delinsGC
ENST00000555020.5:n.1737_1738delinsGC
ENST00000555754.1:n.396_397delinsGC
ENST00000556278.1:c.432+997_432+998delinsGC	ENSP00000451792.1:n.432+997_432+998delins...
ENST00000557706.5:n.1523_1524delinsGC
NM_000155.3:c.948_949delinsGC	NP_000146.2:p.Trp316=
NM_001258332.1:c.621_622delinsGC	NP_001245261.1:p.Trp207=
NM_000155.4:c.948_949delinsGC MANE Select	NP_000146.2:p.Trp316=
NM_001258332.2:c.621_622delinsGC	NP_001245261.1:p.Trp207=