Canonical Allele Identifier: CA374979264

Gene: ST6GALNAC4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127912302C>T , CM000671.2:g.127912302C>T	GRCh38
NC_000009.11:g.130674581C>T , CM000671.1:g.130674581C>T	GRCh37
NC_000009.10:g.129714402C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_175039.4:c.577G>A MANE Select	NP_778204.1:p.Asp193Asn
ENST00000335791.10:c.577G>A MANE Select	ENSP00000336733.5:p.Asp193Asn
NM_175039.3:c.577G>A	NP_778204.1:p.Asp193Asn
NM_175040.3:c.325G>A	NP_778205.1:p.Asp109Asn
NM_175040.4:c.325G>A	NP_778205.1:p.Asp109Asn
NR_174624.1:n.781G>A
NR_174625.1:n.868G>A
ENST00000335791.9:c.577G>A	ENSP00000336733.5:p.Asp193Asn
ENST00000361444.3:c.325G>A	ENSP00000355130.3:p.Asp109Asn
ENST00000467674.5:n.467-2244G>A
ENST00000474282.2:n.93G>A
ENST00000495983.1:n.486G>A
XM_011518527.1:c.646G>A	XP_011516829.1:p.Asp216Asn
XM_011518527.3:c.646G>A	XP_011516829.1:p.Asp216Asn
XM_011518528.1:c.646G>A	XP_011516830.1:p.Asp216Asn
XM_011518529.1:c.646G>A	XP_011516831.1:p.Asp216Asn
XM_011518529.2:c.646G>A	XP_011516831.1:p.Asp216Asn
XM_011518530.1:c.646G>A	XP_011516832.1:p.Asp216Asn
XM_024447518.1:c.577G>A	XP_024303286.1:p.Asp193Asn
XR_002956775.1:n.948G>A
XR_929762.1:n.947G>A