Canonical Allele Identifier: CA395803830

Gene: ABCC11

Linked Data

• MyVariant Identifiers: chr16:g.48201411C>G (hg19) ; chr16:g.48167500C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.48167500C>G , CM000678.2:g.48167500C>G	GRCh38
NC_000016.9:g.48201411C>G , CM000678.1:g.48201411C>G	GRCh37
NC_000016.8:g.46758912C>G	NCBI36
NG_011522.1:g.72678G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356608.7:c.4052G>C MANE Select	ENSP00000349017.2:p.Gly1351Ala
ENST00000353782.9:c.3938G>C	ENSP00000311326.6:p.Gly1313Ala
ENST00000356608.6:c.4052G>C	ENSP00000349017.2:p.Gly1351Ala
ENST00000394747.5:c.4052G>C	ENSP00000378230.1:p.Gly1351Ala
ENST00000394748.5:c.4052G>C	ENSP00000378231.1:p.Gly1351Ala
ENST00000565329.1:n.1352G>C
NM_032583.3:c.4052G>C	NP_115972.2:p.Gly1351Ala
NM_033151.3:c.4052G>C	NP_149163.2:p.Gly1351Ala
NM_145186.2:c.3938G>C	NP_660187.1:p.Gly1313Ala
XM_011523396.1:c.3854G>C	XP_011521698.1:p.Gly1285Ala
XM_011523397.1:c.3095G>C	XP_011521699.1:p.Gly1032Ala
XM_011523398.1:c.2183G>C	XP_011521700.1:p.Gly728Ala
XM_011523397.2:c.3095G>C	XP_011521699.1:p.Gly1032Ala
XM_011523398.3:c.2183G>C	XP_011521700.1:p.Gly728Ala
XM_017023795.2:c.4052G>C	XP_016879284.1:p.Gly1351Ala
XM_017023796.2:c.4052G>C	XP_016879285.1:p.Gly1351Ala
XM_017023797.2:c.4052G>C	XP_016879286.1:p.Gly1351Ala
XM_017023798.2:c.4052G>C	XP_016879287.1:p.Gly1351Ala
XM_017023799.2:c.4052G>C	XP_016879288.1:p.Gly1351Ala
XM_017023800.2:c.4052G>C	XP_016879289.1:p.Gly1351Ala
XM_017023801.2:c.3944G>C	XP_016879290.1:p.Gly1315Ala
XM_017023802.2:c.3095G>C	XP_016879291.1:p.Gly1032Ala
XM_024450475.1:c.3095G>C	XP_024306243.1:p.Gly1032Ala
XR_001752012.1:n.6730G>C
NM_001370496.1:c.4058G>C	NP_001357425.1:p.Gly1353Ala
NM_001370497.1:c.4052G>C MANE Select	NP_001357426.1:p.Gly1351Ala
NM_032583.4:c.4052G>C	NP_115972.2:p.Gly1351Ala
NM_033151.4:c.4052G>C	NP_149163.2:p.Gly1351Ala
NM_145186.3:c.3938G>C	NP_660187.1:p.Gly1313Ala