Canonical Allele Identifier: CA1278105207

Gene: SULT1C4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108378516_108378517delinsAG , CM000664.2:g.108378516_108378517delinsAG	GRCh38
NC_000002.11:g.108994972_108994973delinsAG , CM000664.1:g.108994972_108994973delinsAG	GRCh37
NC_000002.10:g.108361404_108361405delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.169+10_169+11delinsAG MANE Select	ENSP00000272452.2:n.169+10_169+11delinsAG
ENST00000272452.6:c.169+10_169+11delinsAG	ENSP00000272452.2:n.169+10_169+11delinsAG
ENST00000409309.3:c.169+10_169+11delinsAG	ENSP00000387225.3:n.169+10_169+11delinsAG
ENST00000494122.1:n.596+10_596+11delinsAG
NM_006588.2:c.169+10_169+11delinsAG	NP_006579.2:n.169+10_169+11delinsAG
XM_005263919.2:c.169+10_169+11delinsAG	XP_005263976.1:n.169+10_169+11delinsAG
NM_001321770.1:c.169+10_169+11delinsAG	NP_001308699.1:n.169+10_169+11delinsAG
NM_006588.3:c.169+10_169+11delinsAG	NP_006579.2:n.169+10_169+11delinsAG
NR_135776.1:n.596+10_596+11delinsAG
NR_135779.1:n.596+10_596+11delinsAG
XM_017003807.1:c.-152+10_-152+11delinsAG	XP_016859296.1:n.-152+10_-152+11delinsAG
NM_006588.4:c.169+10_169+11delinsAG MANE Select	NP_006579.2:n.169+10_169+11delinsAG
NM_001321770.2:c.169+10_169+11delinsAG	NP_001308699.1:n.169+10_169+11delinsAG
NR_135776.2:n.553+10_553+11delinsAG
NR_135779.2:n.553+10_553+11delinsAG