Canonical Allele Identifier: CA495442675

Gene: ABCC11

Linked Data

• MyVariant Identifiers: chr16:g.48201506T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.48167595T>C , CM000678.2:g.48167595T>C	GRCh38
NC_000016.9:g.48201506T>C , CM000678.1:g.48201506T>C	GRCh37
NC_000016.8:g.46759007T>C	NCBI36
NG_011522.1:g.72583A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356608.7:c.3957A>G MANE Select	ENSP00000349017.2:p.Thr1319=
ENST00000353782.9:c.3843A>G	ENSP00000311326.6:p.Thr1281=
ENST00000356608.6:c.3957A>G	ENSP00000349017.2:p.Thr1319=
ENST00000394747.5:c.3957A>G	ENSP00000378230.1:p.Thr1319=
ENST00000394748.5:c.3957A>G	ENSP00000378231.1:p.Thr1319=
ENST00000565329.1:n.1257A>G
NM_032583.3:c.3957A>G	NP_115972.2:p.Thr1319=
NM_033151.3:c.3957A>G	NP_149163.2:p.Thr1319=
NM_145186.2:c.3843A>G	NP_660187.1:p.Thr1281=
XM_011523396.1:c.3759A>G	XP_011521698.1:p.Thr1253=
XM_011523397.1:c.3000A>G	XP_011521699.1:p.Thr1000=
XM_011523398.1:c.2088A>G	XP_011521700.1:p.Thr696=
XM_011523397.2:c.3000A>G	XP_011521699.1:p.Thr1000=
XM_011523398.3:c.2088A>G	XP_011521700.1:p.Thr696=
XM_017023795.2:c.3957A>G	XP_016879284.1:p.Thr1319=
XM_017023796.2:c.3957A>G	XP_016879285.1:p.Thr1319=
XM_017023797.2:c.3957A>G	XP_016879286.1:p.Thr1319=
XM_017023798.2:c.3957A>G	XP_016879287.1:p.Thr1319=
XM_017023799.2:c.3957A>G	XP_016879288.1:p.Thr1319=
XM_017023800.2:c.3957A>G	XP_016879289.1:p.Thr1319=
XM_017023801.2:c.3849A>G	XP_016879290.1:p.Thr1283=
XM_017023802.2:c.3000A>G	XP_016879291.1:p.Thr1000=
XM_024450475.1:c.3000A>G	XP_024306243.1:p.Thr1000=
XR_001752012.1:n.6635A>G
NM_001370496.1:c.3963A>G	NP_001357425.1:p.Thr1321=
NM_001370497.1:c.3957A>G MANE Select	NP_001357426.1:p.Thr1319=
NM_032583.4:c.3957A>G	NP_115972.2:p.Thr1319=
NM_033151.4:c.3957A>G	NP_149163.2:p.Thr1319=
NM_145186.3:c.3843A>G	NP_660187.1:p.Thr1281=