Canonical Allele Identifier: CA394382832

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2161594C>G (hg19) ; chr16:g.2111593C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2111593C>G , CM000678.2:g.2111593C>G	GRCh38
NC_000016.9:g.2161594C>G , CM000678.1:g.2161594C>G	GRCh37
NC_000016.8:g.2101595C>G	NCBI36
NG_008617.1:g.29306G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.3574G>C MANE Select	ENSP00000262304.4:p.Glu1192Gln
ENST00000262304.8:c.3574G>C	ENSP00000262304.4:p.Glu1192Gln
ENST00000415938.7:n.310+747G>C
ENST00000423118.5:c.3574G>C	ENSP00000399501.1:p.Glu1192Gln
ENST00000468674.5:n.430+747G>C
ENST00000469241.2:n.524G>C
ENST00000483024.1:c.233+223G>C
ENST00000483731.5:n.790+747G>C
ENST00000488185.2:c.473-3235G>C
ENST00000565639.6:n.773+747G>C
ENST00000568591.5:c.2226+747G>C	ENSP00000457162.1:n.2226+747G>C
ENST00000569983.5:n.421+747G>C
NM_000296.3:c.3574G>C	NP_000287.3:p.Glu1192Gln
NM_001009944.2:c.3574G>C	NP_001009944.2:p.Glu1192Gln
XM_005255370.2:c.529G>C	XP_005255427.1:p.Glu177Gln
XM_011522525.1:c.3652G>C	XP_011520827.1:p.Glu1218Gln
XM_011522526.1:c.3652G>C	XP_011520828.1:p.Glu1218Gln
XM_011522527.1:c.3652G>C	XP_011520829.1:p.Glu1218Gln
XM_011522528.1:c.3628G>C	XP_011520830.1:p.Glu1210Gln
XM_011522529.1:c.3628G>C	XP_011520831.1:p.Glu1210Gln
XM_011522530.1:c.3598G>C	XP_011520832.1:p.Glu1200Gln
XM_011522531.1:c.3580G>C	XP_011520833.1:p.Glu1194Gln
XM_011522532.1:c.3526G>C	XP_011520834.1:p.Glu1176Gln
XM_011522533.1:c.3445G>C	XP_011520835.1:p.Glu1149Gln
XM_011522534.1:c.3388G>C	XP_011520836.1:p.Glu1130Gln
XM_011522535.1:c.1474G>C	XP_011520837.1:p.Glu492Gln
XM_011522536.1:c.3652G>C	XP_011520838.1:p.Glu1218Gln
XM_011522537.1:c.652G>C	XP_011520839.1:p.Glu218Gln
XR_932867.1:n.3667G>C
XR_932868.1:n.3667G>C
XR_932869.1:n.3667G>C
XR_932870.1:n.3667G>C
XM_005255370.3:c.529G>C	XP_005255427.1:p.Glu177Gln
XM_011522528.3:c.3628G>C	XP_011520830.1:p.Glu1210Gln
XM_011522529.2:c.3628G>C	XP_011520831.1:p.Glu1210Gln
XM_011522537.2:c.652G>C	XP_011520839.1:p.Glu218Gln
XM_024450298.1:c.3694G>C	XP_024306066.1:p.Glu1232Gln
XM_024450299.1:c.3622G>C	XP_024306067.1:p.Glu1208Gln
XM_024450300.1:c.3484G>C	XP_024306068.1:p.Glu1162Gln
XM_024450301.1:c.1570G>C	XP_024306069.1:p.Glu524Gln
NM_000296.4:c.3574G>C	NP_000287.4:p.Glu1192Gln
NM_001009944.3:c.3574G>C MANE Select	NP_001009944.3:p.Glu1192Gln