Canonical Allele Identifier: CA103392136
Gene: GSTCD HGNC NCBI
INTS12 HGNC NCBI

Linked Data

dbSNP Id: rs10516526

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105767747A>G , CM000666.2:g.105767747A>G GRCh38
NC_000004.11:g.106688904A>G , CM000666.1:g.106688904A>G GRCh37
NC_000004.10:g.106908353A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000515279.6:c.1240+38248A>G (GSTCD) MANE Select ENSP00000422354.1:n.1240+38248A>G
ENST00000360505.9:c.1240+38248A>G (GSTCD) ENSP00000353695.5:n.1240+38248A>G
ENST00000394728.4:c.1240+38248A>G (GSTCD) ENSP00000378216.3:n.1240+38248A>G
ENST00000394730.7:c.979+38248A>G (GSTCD) ENSP00000378218.3:n.979+38248A>G
ENST00000484843.1:n.1491+38248A>G (GSTCD)
ENST00000510876.1:c.31-67733T>C (INTS12) ENSP00000422856.1:n.31-67733T>C
ENST00000515255.5:n.579+38248A>G (GSTCD)
ENST00000515279.5:c.1240+38248A>G (GSTCD) ENSP00000422354.1:n.1240+38248A>G
NM_001031720.3:c.1240+38248A>G (GSTCD) NP_001026890.2:n.1240+38248A>G
NM_024751.3:c.979+38248A>G (GSTCD) NP_079027.2:n.979+38248A>G
XM_005263222.2:c.1240+38248A>G (GSTCD) XP_005263279.1:n.1240+38248A>G
XM_011532248.1:c.1240+38248A>G (GSTCD) XP_011530550.1:n.1240+38248A>G
XM_011532249.1:c.1240+38248A>G (GSTCD) XP_011530551.1:n.1240+38248A>G
XM_011532250.1:c.1240+38248A>G (GSTCD) XP_011530552.1:n.1240+38248A>G
XM_011532251.1:c.1240+38248A>G (GSTCD) XP_011530553.1:n.1240+38248A>G
XM_011532252.1:c.1240+38248A>G (GSTCD) XP_011530554.1:n.1240+38248A>G
XR_244687.2:n.1191-14446T>C
XR_938771.1:n.1500+38248A>G (GSTCD)
XM_005263222.4:c.1240+38248A>G (GSTCD) XP_005263279.1:n.1240+38248A>G
XM_011532248.3:c.1240+38248A>G (GSTCD) XP_011530550.1:n.1240+38248A>G
XM_011532249.3:c.1240+38248A>G (GSTCD) XP_011530551.1:n.1240+38248A>G
XM_011532252.3:c.1240+38248A>G (GSTCD) XP_011530554.1:n.1240+38248A>G
NM_001370181.1:c.1240+38248A>G (GSTCD) MANE Select NP_001357110.1:n.1240+38248A>G