Canonical Allele Identifier: CA394393037

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2167824C>G (hg19) ; chr16:g.2117823C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2117823C>G , CM000678.2:g.2117823C>G	GRCh38
NC_000016.9:g.2167824C>G , CM000678.1:g.2167824C>G	GRCh37
NC_000016.8:g.2107825C>G	NCBI36
NG_008617.1:g.23076G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262304.9:c.1169G>C MANE Select	ENSP00000262304.4:p.Ser390Thr
ENST00000262304.8:c.1169G>C	ENSP00000262304.4:p.Ser390Thr
ENST00000423118.5:c.1169G>C	ENSP00000399501.1:p.Ser390Thr
ENST00000488185.2:c.256G>C
ENST00000568591.5:c.137G>C	ENSP00000457162.1:p.Ser46Thr
ENST00000570150.1:n.302G>C
NM_000296.3:c.1169G>C	NP_000287.3:p.Ser390Thr
NM_001009944.2:c.1169G>C	NP_001009944.2:p.Ser390Thr
XM_011522525.1:c.1223G>C	XP_011520827.1:p.Ser408Thr
XM_011522526.1:c.1223G>C	XP_011520828.1:p.Ser408Thr
XM_011522527.1:c.1223G>C	XP_011520829.1:p.Ser408Thr
XM_011522528.1:c.1223G>C	XP_011520830.1:p.Ser408Thr
XM_011522529.1:c.1223G>C	XP_011520831.1:p.Ser408Thr
XM_011522530.1:c.1169G>C	XP_011520832.1:p.Ser390Thr
XM_011522531.1:c.1151G>C	XP_011520833.1:p.Ser384Thr
XM_011522532.1:c.1097G>C	XP_011520834.1:p.Ser366Thr
XM_011522533.1:c.1016G>C	XP_011520835.1:p.Ser339Thr
XM_011522534.1:c.959G>C	XP_011520836.1:p.Ser320Thr
XM_011522536.1:c.1223G>C	XP_011520838.1:p.Ser408Thr
XR_932867.1:n.1238G>C
XR_932868.1:n.1238G>C
XR_932869.1:n.1238G>C
XR_932870.1:n.1238G>C
XM_011522528.3:c.1223G>C	XP_011520830.1:p.Ser408Thr
XM_011522529.2:c.1223G>C	XP_011520831.1:p.Ser408Thr
XM_024450298.1:c.1169G>C	XP_024306066.1:p.Ser390Thr
XM_024450299.1:c.1097G>C	XP_024306067.1:p.Ser366Thr
XM_024450300.1:c.959G>C	XP_024306068.1:p.Ser320Thr
NM_000296.4:c.1169G>C	NP_000287.4:p.Ser390Thr
NM_001009944.3:c.1169G>C MANE Select	NP_001009944.3:p.Ser390Thr