Canonical Allele Identifier: CA493049594

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2164450C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2114449C>G , CM000678.2:g.2114449C>G	GRCh38
NC_000016.9:g.2164450C>G , CM000678.1:g.2164450C>G	GRCh37
NC_000016.8:g.2104451C>G	NCBI36
NG_008617.1:g.26450G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.2574G>C MANE Select	ENSP00000262304.4:p.Thr858=
ENST00000262304.8:c.2574G>C	ENSP00000262304.4:p.Thr858=
ENST00000423118.5:c.2574G>C	ENSP00000399501.1:p.Thr858=
ENST00000488185.2:c.472+3040G>C
ENST00000565639.6:n.33G>C
ENST00000568591.5:c.1505G>C	ENSP00000457162.1:n.1505G>C
NM_000296.3:c.2574G>C	NP_000287.3:p.Thr858=
NM_001009944.2:c.2574G>C	NP_001009944.2:p.Thr858=
XM_011522525.1:c.2628G>C	XP_011520827.1:p.Thr876=
XM_011522526.1:c.2628G>C	XP_011520828.1:p.Thr876=
XM_011522527.1:c.2628G>C	XP_011520829.1:p.Thr876=
XM_011522528.1:c.2628G>C	XP_011520830.1:p.Thr876=
XM_011522529.1:c.2628G>C	XP_011520831.1:p.Thr876=
XM_011522530.1:c.2574G>C	XP_011520832.1:p.Thr858=
XM_011522531.1:c.2556G>C	XP_011520833.1:p.Thr852=
XM_011522532.1:c.2502G>C	XP_011520834.1:p.Thr834=
XM_011522533.1:c.2421G>C	XP_011520835.1:p.Thr807=
XM_011522534.1:c.2364G>C	XP_011520836.1:p.Thr788=
XM_011522535.1:c.450G>C	XP_011520837.1:p.Thr150=
XM_011522536.1:c.2628G>C	XP_011520838.1:p.Thr876=
XR_932867.1:n.2643G>C
XR_932868.1:n.2643G>C
XR_932869.1:n.2643G>C
XR_932870.1:n.2643G>C
XM_005255370.3:c.-476G>C	XP_005255427.1:n.-476G>C
XM_011522528.3:c.2628G>C	XP_011520830.1:p.Thr876=
XM_011522529.2:c.2628G>C	XP_011520831.1:p.Thr876=
XM_024450298.1:c.2574G>C	XP_024306066.1:p.Thr858=
XM_024450299.1:c.2502G>C	XP_024306067.1:p.Thr834=
XM_024450300.1:c.2364G>C	XP_024306068.1:p.Thr788=
XM_024450301.1:c.450G>C	XP_024306069.1:p.Thr150=
NM_000296.4:c.2574G>C	NP_000287.4:p.Thr858=
NM_001009944.3:c.2574G>C MANE Select	NP_001009944.3:p.Thr858=