Canonical Allele Identifier: CA15841956

Gene: PIAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68175422G>C , CM000677.2:g.68175422G>C	GRCh38
NC_000015.9:g.68467760G>C , CM000677.1:g.68467760G>C	GRCh37
NC_000015.8:g.66254814G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016166.3:c.1170-215G>C MANE Select	NP_057250.1:n.1170-215G>C
ENST00000249636.11:c.1170-215G>C MANE Select	ENSP00000249636.6:n.1170-215G>C
NM_001320687.1:c.1176-215G>C	NP_001307616.1:n.1176-215G>C
NM_016166.1:c.1170-215G>C	NP_057250.1:n.1170-215G>C
NM_016166.2:c.1170-215G>C	NP_057250.1:n.1170-215G>C
ENST00000249636.10:c.1170-215G>C	ENSP00000249636.6:n.1170-215G>C
ENST00000545237.1:c.1176-215G>C	ENSP00000438574.1:n.1176-215G>C
XM_005254735.1:c.1143-215G>C	XP_005254792.1:n.1143-215G>C
XM_011522126.1:c.1197-215G>C	XP_011520428.1:n.1197-215G>C
XM_011522126.2:c.1197-215G>C	XP_011520428.1:n.1197-215G>C
XM_011522127.1:c.1152-215G>C	XP_011520429.1:n.1152-215G>C
XM_011522127.2:c.1152-215G>C	XP_011520429.1:n.1152-215G>C
XM_011522128.1:c.1143-215G>C	XP_011520430.1:n.1143-215G>C
XM_017022688.1:c.1176-215G>C	XP_016878177.1:n.1176-215G>C
XM_017022689.1:c.1149-215G>C	XP_016878178.1:n.1149-215G>C
XM_017022690.1:c.1143-215G>C	XP_016878179.1:n.1143-215G>C
XM_017022691.2:c.1143-215G>C	XP_016878180.1:n.1143-215G>C
XM_024450094.1:c.618-215G>C	XP_024305862.1:n.618-215G>C