Canonical Allele Identifier: CA119085

Gene: GALNT3

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165759443A>C , CM000664.2:g.165759443A>C	GRCh38
NC_000002.11:g.166615953A>C , CM000664.1:g.166615953A>C	GRCh37
NC_000002.10:g.166324199A>C	NCBI36
NG_012069.1:g.39851T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392701.8:c.966T>G MANE Select	ENSP00000376465.3:p.Tyr322Ter
ENST00000392701.7:c.966T>G	ENSP00000376465.3:p.Tyr322Ter
ENST00000409882.5:c.180T>G	ENSP00000386955.1:p.Tyr60Ter
ENST00000412248.5:c.966T>G	ENSP00000412643.1:p.Tyr322Ter
ENST00000437849.1:c.394T>G	ENSP00000391104.1:n.394T>G
ENST00000463254.1:n.249T>G
NM_004482.3:c.966T>G	NP_004473.2:p.Tyr322Ter
XM_005246449.1:c.966T>G	XP_005246506.1:p.Tyr322Ter
XM_006712402.2:c.966T>G	XP_006712465.1:p.Tyr322Ter
XM_011510929.1:c.966T>G	XP_011509231.1:p.Tyr322Ter
XM_017003770.1:c.966T>G	XP_016859259.1:p.Tyr322Ter
XR_002959253.1:n.1307T>G
NM_004482.4:c.966T>G MANE Select	NP_004473.2:p.Tyr322Ter