Canonical Allele Identifier: CA395803937

Gene: ABCC11

Linked Data

• MyVariant Identifiers: chr16:g.48201424C>G (hg19) ; chr16:g.48167513C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.48167513C>G , CM000678.2:g.48167513C>G	GRCh38
NC_000016.9:g.48201424C>G , CM000678.1:g.48201424C>G	GRCh37
NC_000016.8:g.46758925C>G	NCBI36
NG_011522.1:g.72665G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356608.7:c.4039G>C MANE Select	ENSP00000349017.2:p.Val1347Leu
ENST00000353782.9:c.3925G>C	ENSP00000311326.6:p.Val1309Leu
ENST00000356608.6:c.4039G>C	ENSP00000349017.2:p.Val1347Leu
ENST00000394747.5:c.4039G>C	ENSP00000378230.1:p.Val1347Leu
ENST00000394748.5:c.4039G>C	ENSP00000378231.1:p.Val1347Leu
ENST00000565329.1:n.1339G>C
NM_032583.3:c.4039G>C	NP_115972.2:p.Val1347Leu
NM_033151.3:c.4039G>C	NP_149163.2:p.Val1347Leu
NM_145186.2:c.3925G>C	NP_660187.1:p.Val1309Leu
XM_011523396.1:c.3841G>C	XP_011521698.1:p.Val1281Leu
XM_011523397.1:c.3082G>C	XP_011521699.1:p.Val1028Leu
XM_011523398.1:c.2170G>C	XP_011521700.1:p.Val724Leu
XM_011523397.2:c.3082G>C	XP_011521699.1:p.Val1028Leu
XM_011523398.3:c.2170G>C	XP_011521700.1:p.Val724Leu
XM_017023795.2:c.4039G>C	XP_016879284.1:p.Val1347Leu
XM_017023796.2:c.4039G>C	XP_016879285.1:p.Val1347Leu
XM_017023797.2:c.4039G>C	XP_016879286.1:p.Val1347Leu
XM_017023798.2:c.4039G>C	XP_016879287.1:p.Val1347Leu
XM_017023799.2:c.4039G>C	XP_016879288.1:p.Val1347Leu
XM_017023800.2:c.4039G>C	XP_016879289.1:p.Val1347Leu
XM_017023801.2:c.3931G>C	XP_016879290.1:p.Val1311Leu
XM_017023802.2:c.3082G>C	XP_016879291.1:p.Val1028Leu
XM_024450475.1:c.3082G>C	XP_024306243.1:p.Val1028Leu
XR_001752012.1:n.6717G>C
NM_001370496.1:c.4045G>C	NP_001357425.1:p.Val1349Leu
NM_001370497.1:c.4039G>C MANE Select	NP_001357426.1:p.Val1347Leu
NM_032583.4:c.4039G>C	NP_115972.2:p.Val1347Leu
NM_033151.4:c.4039G>C	NP_149163.2:p.Val1347Leu
NM_145186.3:c.3925G>C	NP_660187.1:p.Val1309Leu