Canonical Allele Identifier: CA1845635693

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647211_34647219delinsGACCCTCTC , CM000671.2:g.34647211_34647219delinsGACCCTCTC	GRCh38
NC_000009.11:g.34647208_34647216delinsGACCCTCTC , CM000671.1:g.34647208_34647216delinsGACCCTCTC	GRCh37
NC_000009.10:g.34637208_34637216delinsGACCCTCTC	NCBI36
NG_009029.1:g.5574_5582delinsGACCCTCTC
NG_028966.1:g.27_35delinsGACCCTCTC
NG_009029.2:g.5623_5631delinsGACCCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.205_213delinsGACCCTCTC	ENSP00000509954.1:p.Asp69=
ENST00000378842.8:c.205_213delinsGACCCTCTC MANE Select	ENSP00000368119.4:p.Asp69=
ENST00000378842.7:c.205_213delinsGACCCTCTC	ENSP00000368119.3:p.Asp69=
ENST00000450095.6:c.3_11delinsGACCCTCTC	ENSP00000401956.2:p.Met1=
ENST00000465543.6:n.544_552delinsGACCCTCTC
ENST00000468099.2:n.245_253delinsGACCCTCTC
ENST00000472111.5:n.246_254delinsGACCCTCTC
ENST00000473506.6:c.205_213delinsGACCCTCTC	ENSP00000432839.2:p.Asp69=
ENST00000473529.5:n.252_260delinsGACCCTCTC
ENST00000485531.1:n.198_206delinsGACCCTCTC
ENST00000487381.5:n.231_239delinsGACCCTCTC
ENST00000489643.6:n.235_243delinsGACCCTCTC
ENST00000554085.5:c.205_213delinsGACCCTCTC	ENSP00000450419.1:p.Asp69=
ENST00000554139.5:n.258_266delinsGACCCTCTC
ENST00000554330.5:n.202_210delinsGACCCTCTC
ENST00000554550.5:c.205_213delinsGACCCTCTC	ENSP00000451435.1:p.Asp69=
ENST00000554638.5:n.229_237delinsGACCCTCTC
ENST00000554897.5:c.205_213delinsGACCCTCTC	ENSP00000450942.1:p.Asp69=
ENST00000554944.5:n.235_243delinsGACCCTCTC
ENST00000555020.5:n.235_243delinsGACCCTCTC
ENST00000555086.5:n.209_217delinsGACCCTCTC
ENST00000555214.5:n.214_222delinsGACCCTCTC
ENST00000556157.1:n.312_320delinsGACCCTCTC
ENST00000556244.1:c.89_97delinsGACCCTCTC
ENST00000556278.1:c.205_213delinsGACCCTCTC	ENSP00000451792.1:p.Asp69=
ENST00000556403.5:n.218_226delinsGACCCTCTC
ENST00000556494.5:n.237_245delinsGACCCTCTC
ENST00000557541.5:n.398_406delinsGACCCTCTC
ENST00000557706.5:n.319_327delinsGACCCTCTC
NM_000155.3:c.205_213delinsGACCCTCTC	NP_000146.2:p.Asp69=
NM_001258332.1:c.3_11delinsGACCCTCTC	NP_001245261.1:p.Met1=
NM_000155.4:c.205_213delinsGACCCTCTC MANE Select	NP_000146.2:p.Asp69=
NM_001258332.2:c.3_11delinsGACCCTCTC	NP_001245261.1:p.Met1=