Canonical Allele Identifier: CA1304729803
Gene: GALNT3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165751206C= , CM000664.2:g.165751206C= GRCh38
NC_000002.11:g.166607716C= , CM000664.1:g.166607716C= GRCh37
NC_000002.10:g.166315962C= NCBI36
NG_012069.1:g.48088G=

Transcript Alleles

HGVS Amino-acid change
ENST00000392701.8:c.1627-1312G= MANE Select ENSP00000376465.3:n.1627-1312G=
ENST00000392701.7:c.1627-1312G= ENSP00000376465.3:n.1627-1312G=
ENST00000409882.5:c.841-1312G= ENSP00000386955.1:n.841-1312G=
NM_004482.3:c.1627-1312G= NP_004473.2:n.1627-1312G=
XM_005246449.1:c.1627-1312G= XP_005246506.1:n.1627-1312G=
XM_011510929.1:c.1627-1312G= XP_011509231.1:n.1627-1312G=
XM_017003770.1:c.1627-1312G= XP_016859259.1:n.1627-1312G=
XR_002959253.1:n.1903-1312G=
NM_004482.4:c.1627-1312G= MANE Select NP_004473.2:n.1627-1312G=
Search 100 bp 5'
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