Canonical Allele Identifier: CA863494873

Gene: GALT

Linked Data

• dbSNP Id: rs1370245469
• MyVariant Identifiers: chr9:g.34647387G>C (hg19) ; chr9:g.34647390G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647390G>C , CM000671.2:g.34647390G>C	GRCh38
NC_000009.11:g.34647387G>C , CM000671.1:g.34647387G>C	GRCh37
NC_000009.10:g.34637387G>C	NCBI36
NG_009029.1:g.5753G>C
NG_028966.1:g.206G>C
NG_009029.2:g.5802G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.253-102G>C	ENSP00000509954.1:n.253-102G>C
ENST00000378842.8:c.253-102G>C MANE Select	ENSP00000368119.4:n.253-102G>C
ENST00000378842.7:c.253-102G>C	ENSP00000368119.3:n.253-102G>C
ENST00000450095.6:c.50+132G>C	ENSP00000401956.2:n.50+132G>C
ENST00000465543.6:n.592-102G>C
ENST00000468099.2:n.424G>C
ENST00000472111.5:n.294-102G>C
ENST00000473506.6:c.252+132G>C	ENSP00000432839.2:n.252+132G>C
ENST00000473529.5:n.300-102G>C
ENST00000485531.1:n.377G>C
ENST00000487381.5:n.410G>C
ENST00000489643.6:n.282+132G>C
ENST00000554085.5:c.253-85G>C	ENSP00000450419.1:n.253-85G>C
ENST00000554139.5:n.306-102G>C
ENST00000554330.5:n.249+132G>C
ENST00000554550.5:c.252+132G>C	ENSP00000451435.1:n.252+132G>C
ENST00000554638.5:n.408G>C
ENST00000554897.5:c.252+132G>C	ENSP00000450942.1:n.252+132G>C
ENST00000554944.5:n.282+132G>C
ENST00000555020.5:n.283-102G>C
ENST00000555086.5:n.257-102G>C
ENST00000555214.5:n.261+132G>C
ENST00000556157.1:n.360-85G>C
ENST00000556244.1:c.138G>C
ENST00000556278.1:c.252+132G>C	ENSP00000451792.1:n.252+132G>C
ENST00000556403.5:n.266-102G>C
ENST00000556494.5:n.285-102G>C
ENST00000557541.5:n.445+132G>C
ENST00000557706.5:n.498G>C
NM_000155.3:c.253-102G>C	NP_000146.2:n.253-102G>C
NM_001258332.1:c.50+132G>C	NP_001245261.1:n.50+132G>C
NM_000155.4:c.253-102G>C MANE Select	NP_000146.2:n.253-102G>C
NM_001258332.2:c.50+132G>C	NP_001245261.1:n.50+132G>C