Canonical Allele Identifier: CA1304746901

Gene: GALNT3

Linked Data

• dbSNP Id: rs4621175

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165792282A>G , CM000664.2:g.165792282A>G	GRCh38
NC_000002.11:g.166648792A>G , CM000664.1:g.166648792A>G	GRCh37
NC_000002.10:g.166357038A>G	NCBI36
NG_012069.1:g.7012T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000392701.8:c.-109+1733T>C MANE Select	ENSP00000376465.3:n.-109+1733T>C
ENST00000392701.7:c.-109+1733T>C	ENSP00000376465.3:n.-109+1733T>C
ENST00000412248.5:c.-228+2043T>C	ENSP00000412643.1:n.-228+2043T>C
ENST00000414977.5:c.-228+1438T>C	ENSP00000413477.1:n.-228+1438T>C
ENST00000422973.1:c.-228+1733T>C	ENSP00000413694.1:n.-228+1733T>C
ENST00000431484.1:c.-109+2207T>C	ENSP00000397112.1:n.-109+2207T>C
NM_004482.3:c.-109+1733T>C	NP_004473.2:n.-109+1733T>C
XM_006712402.2:c.-109+1733T>C	XP_006712465.1:n.-109+1733T>C
XM_011510929.1:c.-109+2207T>C	XP_011509231.1:n.-109+2207T>C
XM_017003770.1:c.-109+2043T>C	XP_016859259.1:n.-109+2043T>C
XR_002959253.1:n.233+1733T>C
NM_004482.4:c.-109+1733T>C MANE Select	NP_004473.2:n.-109+1733T>C